International Statistical Classification of Diseases and Related Health Problems 10th

Revision
Chapter Blocks Title
I A00-B99 Certain infectious and parasitic diseases
II C00-D48 Neoplasms
D50- Diseases of the blood and blood-forming organs and certain disorders
III
D89 involving the immune mechanism
IV E00-E90 Endocrine, nutritional and metabolic diseases
V F00-F99 Mental and behavioural disorders
G00-
VI Diseases of the nervous system
G99
H00-
VII Diseases of the eye and adnexa
H59
H60-
VIII Diseases of the ear and mastoid process
H95
IX I00-I99 Diseases of the circulatory system
X J00-J99 Diseases of the respiratory system
K00-
XI Diseases of the digestive system
K93
XII L00-L99 Diseases of the skin and subcutaneous tissue
M00-
XIII Diseases of the musculoskeletal system and connective tissue
M99
N00-
XIV Diseases of the genitourinary system
N99
O00-
XV Pregnancy, childbirth and the puerperium
O99
XVI P00-P96 Certain conditions originating in the perinatal period
Q00- Congenital malformations, deformations and chromosomal
XVII
Q99 abnormalities
Symptoms, signs and abnormal clinical and laboratory findings, not
XVIII R00-R99
elsewhere classified
XIX S00-T98 Injury, poisoning and certain other consequences of external causes
V01-
XX External causes of morbidity and mortality
Y98
XXI Z00-Z99 Factors influencing health status and contact with health services
U00-
XXII Codes for special purposes
U99

ICD-10 Chapter I: Certain infectious and

parasitic diseases
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The International Statistical Classification of Diseases and Related Health Problems 10th
Revision (ICD-10) is a coding of diseases and signs, symptoms, abnormal findings,
complaints, social circumstances and external causes of injury or diseases, as classified
by the World Health Organization (WHO).[1]. This page contains ICD-10 Chapter I:
Certain infectious and parasitic diseases.

Contents
[hide]
• 1 A00-A79 - Bacterial infections, and other intestinal infectious diseases, and
STDs
○ 1.1 (A00-A09) Intestinal infectious diseases
○ 1.2 (A15-A19) Tuberculosis
○ 1.3 (A20-A28) Certain zoonotic bacterial diseases
○ 1.4 (A30-A49) Other bacterial diseases
○ 1.5 (A50-A64) Infections with a predominantly sexual mode of
transmission
○ 1.6 (A65-A69) Other spirochaetal diseases
○ 1.7 (A70-A74) Other diseases caused by chlamydiae
○ 1.8 (A75-A79) Rickettsioses
• 2 A80-B34 - Viral infections
○ 2.1 (A80-A89) Viral infections of the central nervous system
○ 2.2 (A90-A99) Arthropod-borne viral fevers and viral haemorrhagic fevers
○ 2.3 (B00-B09) Viral infections characterized by skin and mucous
membrane lesions
○ 2.4 (B15-B19) Viral hepatitis
○ 2.5 (B20-B24) Human immunodeficiency virus (HIV) disease
○ 2.6 (B25-B34) Other viral diseases
• 3 B35-B89 - Infections caused by fungi, protozoans, worms, and infestations
○ 3.1 (B35-B49) Mycoses
○ 3.2 (B50-B64) Protozoal diseases
○ 3.3 (B65-B83) Helminthiases
○ 3.4 (B85-B89) Pediculosis, acariasis and other infestations
• 4 B90-B99 - Sequelae, and diseases classified elsewhere
○ 4.1 (B90-B94) Sequelae of infectious and parasitic diseases
○ 4.2 (B95-B97) Bacterial, viral and other infectious agents
○ 4.3 (B99) Other infectious diseases
• 5 See also
• 6 References
[edit] A00-A79 - Bacterial infections, and other
intestinal infectious diseases, and STDs
[edit] (A00-A09) Intestinal infectious diseases
• (A00.) Cholera
• (A01.) Typhoid and paratyphoid fevers
○ (A01.0) Typhoid fever
 Infection due to Salmonella typhi
○ (A01.1) Paratyphoid fever A
○ (A01.2) Paratyphoid fever B
○ (A01.3) Paratyphoid fever C
○ (A01.4) Paratyphoid fever, unspecified
• (A02.) Other Salmonella infections
• (A03.) Shigellosis
○ (A03.0) Shigellosis due to Shigella dysenteriae
○ (A03.1) Shigellosis due to Shigella flexneri
○ (A03.2) Shigellosis due to Shigella boydii
○ (A03.3) Shigellosis due to Shigella sonnei
○ (A03.8) Other shigellosis
○ (A03.9) Shigellosis, unspecified
 Bacillary dysentery NOS
• (A04.) Other bacterial intestinal infections
•
○ (A04.0) Enteropathogenic Escherichia coli infection
○ (A04.1) Enterotoxigenic Escherichia coli infection
○ (A04.2) Enteroinvasive Escherichia coli infection
○ (A04.3) Enterohaemorrhagic Escherichia coli infection
○ (A04.4) Other intestinal Escherichia coli infections
○ (A04.5) Campylobacter enteritis
○ (A04.6) Enteritis due to Yersinia enterocolitica
○ (A04.7) Enterocolitis due to Clostridium difficile
 Pseudomembranous colitis
○ (A04.8) Other specified bacterial intestinal infections
○ (A04.9) Bacterial intestinal infection, unspecified
 Bacterial enteritis NOS
• (A05.) Other bacterial foodborne intoxications
○ (A05.0) Foodborne staphylococcal intoxication
 ○ (A05.1) Botulism
○ (A05.2) Foodborne Clostridium perfringens (Clostridium welchii)
intoxication
• (A06.) Amoebiasis
○ (A06.0) Acute amoebic dysentery
○ (A06.1) Chronic intestinal amoebiasis
○ (A06.2) Amoebic nondysenteric colitis
○ (A06.3) Amoeboma of intestine
○ (A06.4) Amoebic liver abscess
○ (A06.5) Amoebic lung abscess
○ (A06.6) Amoebic brain abscess
○ (A06.7) Cutaneous amoebiasis
○ (A06.8) Amoebic infection of other sites
○ (A06.9) Amoebiasis, unspecified
• (A07.) Other protozoal intestinal disease
○ (A07.0) Balantidiasis
○ (A07.1) Giardiasis (lambliasis)
○ (A07.2) Cryptosporidiosis
○ (A07.3) Isosporiasis
○ (A07.8) Other specified protozoal intestinal diseases
 Intestinal trichomoniasis
 Sarcocystosis
 Sarcosporidiosis
○ (A07.9) Protozoal intestinal disease, unspecified
• (A08.) Viral and other specified intestinal infections
○ (A08.0) Rotaviral enteritis
• (A09.) Diarrhoea and gastroenteritis of presumed infectious origin
[edit] (A15-A19) Tuberculosis
• (A15.) Respiratory tuberculosis, bacteriologically and histologically confirmed
• (A16.) Respiratory tuberculosis, not confirmed bacteriologically or histologically
• (A17.) Tuberculosis of nervous system
○ (A17.0) Tuberculous meningitis
○ (A17.1) Meningeal tuberculoma
○ (A17.8) Other tuberculosis of nervous system
○ (A17.9) Tuberculosis of nervous system, unspecified
• (A18.) Tuberculosis of other organs
○ (A18.0) Tuberculosis of bones and joints
 ○ (A18.1) Tuberculosis of genitourinary system
○ (A18.2) Tuberculous peripheral lymphadenopathy
○ (A18.3) Tuberculosis of intestines, peritoneum and mesenteric glands
○ (A18.4) Tuberculosis of skin and subcutaneous tissue
 Scrofuloderma
○ (A18.5) Tuberculosis of eye
○ (A18.6) Tuberculosis of ear
○ (A18.7) Tuberculosis of adrenal glands
○ (A18.8) Tuberculosis of other specified organs
• (A19.) Miliary tuberculosis
[edit] (A20-A28) Certain zoonotic bacterial diseases
• (A20.) Plague
○ (A20.0) Bubonic plague
○ (A20.1) Cellulocutaneous plague
○ (A20.2) Pneumonic plague
○ (A20.3) Plague meningitis
○ (A20.7) Septicaemic plague
○ (A20.8) Other forms of plague
○ (A20.9) Plague, unspecified
• (A21.) Tularaemia
• (A22.) Anthrax
• (A23.) Brucellosis
• (A24.) Glanders and melioidosis
○ (A24.0) Glanders
○ (A24.1) acute and fulminating melioidosis
○ (A24.2) Subacute and chronic melioidosis
○ (A24.3) Other melioidosis
○ (A24.4) Melioidosis, unspecified
 Whitmore's disease
• (A25.) Rat-bite fevers
○ (A25.0) Spirillosis
 Sodoku
○ (A25.1) Streptobacillosis
○ (A25.9) Rat-bite fever, unspecified
• (A26.) Erysipeloid
• (A27.) Leptospirosis
• (A28.) Other zoonotic bacterial diseases, not elsewhere classified
 ○ (A28.0) Pasteurellosis
○ (A28.1) Cat-scratch disease
[edit] (A30-A49) Other bacterial diseases
• (A30.) Leprosy (Hansen's disease)
• (A31.) Infection due to other mycobacteria
○ (A31.0) Pulmonary mycobacterial infection
 Infection due to Mycobacterium avium
 Infection due to Mycobacterium intracellulare (Battey bacillus)
 Infection due to Mycobacterium kansasii
○ (A31.1) Cutaneous mycobacterial infection
 Buruli ulcer
 Infection due to Mycobacterium marinum
 Infection due to Mycobacterium ulcerans
○ (A31.8) Other mycobacterial infections
○ (A31.9) Mycobacterial infection, unspecified
 Atypical mycobacterium infection NOS
 Mycobacteriosis NOS
• (A32.) Listeriosis
• (A33.) Tetanus neonatorum
• (A34.) Obstetrical tetanus
• (A35.) Other tetanus
• (A36.) Diphtheria
• (A37.) Whooping cough
• (A38.) Scarlet fever
• (A39.) Meningococcal infection
○ (A39.0) Meningococcal meningitis
○ (A39.1) Waterhouse-Friderichsen syndrome
○ (A39.2) Acute meningococcaemia
○ (A39.3) Chronic meningococcaemia
○ (A39.4) Meningococcaemia, unspecified
○ (A39.5) Meningococcal heart disease
• (A40.) Streptococcal septicaemia
• (A41.) Other septicaemia
○ (A41.0) Septicaemia due to Staphylococcus aureus
○ (A41.1) Septicaemia due to other specified staphylococcus
○ (A41.2) Septicaemia due to unspecified staphylococcus
○ (A41.3) Septicaemia due to Haemophilus influenzae
 ○ (A41.4) Septicaemia due to anaerobes
○ (A41.5) Septicaemia due to other Gram-negative organisms
○ (A41.8) Other specified septicaemia
○ (A41.9) Septicaemia, unspecified
 Septic shock
• (A42.) Actinomycosis
• (A43.) Nocardiosis
• (A44.) Bartonellosis
○ (A44.0) Systemic bartonellosis
○ (A44.1) Cutaneous and mucocutaneous bartonellosis
○ (A44.8) Other forms of bartonellosis
○ (A44.9) Bartonellosis, unspecified
• (A46.) Erysipelas
• (A48.) Other bacterial diseases, not elsewhere classified
○ (A48.0) Gas gangrene
○ (A48.1) Legionnaires' disease
○ (A48.2) Nonpneumonic Legionnaires' disease
○ (A48.3) Toxic shock syndrome
○ (A48.4) Brazilian purpuric fever
○ (A48.8) Other specified bacterial diseases
• (A49.) Bacterial infection of unspecified site
○ (A49.0) Staphylococcal infection, unspecified
○ (A49.1) Streptococcal infection, unspecified
○ (A49.2) Haemophilus influenzae infection, unspecified
○ (A49.3) Mycoplasma infection, unspecified
○ (A49.8) Other bacterial infections of unspecified site
○ (A49.9) Bacterial infection, unspecified
 Bacteraemia NOS
[edit] (A50-A64) Infections with a predominantly sexual mode of
transmission
• (A50.) Congenital syphilis
○ (A50.0) Early congenital syphilis, symptomatic
○ (A50.1) Early congenital syphilis, latent
○ (A50.2) Early congenital syphilis, unspecified
○ (A50.3) Late congenital syphilitic oculopathy
○ (A50.4) Late congenital neurosyphilis (juvenile neurosyphilis)
○ (A50.5) Other late congenital syphilis, symptomatic
 ○ (A50.6) Late congenital syphilis, latent
○ (A50.7) Late congenital syphilis, unspecified
○ (A50.9) Congenital syphilis, unspecified
• (A51.) Early syphilis
○ (A51.0) Primary genital syphilis
 Syphilitic chancre NOS
○ (A51.1) Primary anal syphilis
○ (A51.2) Primary syphilis of other sites
○ (A51.3) Secondary syphilis of skin and mucous membranes
 Condyloma latum
○ (A51.4) Other secondary syphilis
○ (A51.5) Early syphilis, latent
○ (A51.9) Early syphilis, unspecified
• (A52.) Late syphilis
○ (A52.0) Cardiovascular syphilis
○ (A52.1) Symptomatic neurosyphilis
 Tabes dorsalis
○ (A52.2) Asymptomatic neurosyphilis
○ (A52.3) Neurosyphilis, unspecified
 Gumma (syphilitic) of central nervous system NOS
 Syphilis (late) of central nervous system NOS
 Syphiloma of central nervous system NOS
○ (A52.7) Other symptomatic late syphilis
 Gumma (syphilitic) any sites, except those classified to A52.0-
A52.3
 Late or tertiary syphilis any sites, except those classified to A52.0-
A52.3
○ (A52.8) Late syphilis, latent
○ (A52.9) Late syphilis, unspecified
• (A53.) Other and unspecified syphilis
○ (A53.0) Latent syphilis, unspecified as early or late
○ (A53.9) Syphilis, unspecified
• (A54.) Gonococcal infection
○ (A54.0) Gonococcal infection of lower genitourinary tract without
periurethral or accessory gland abscess
○ (A54.1) Gonococcal infection of lower genitourinary tract with
periurethral and accessory gland abscess
 ○ (A54.2) Gonococcal pelviperitonitis and other gonococcal genitourinary
infections
○ (A54.3) Gonococcal infection of eye
○ (A54.4) Gonococcal infection of musculoskeletal system
○ (A54.5) Gonococcal pharyngitis
○ (A54.6) Gonococcal infection of anus and rectum
○ (A54.8) Other gonococcal infections
○ (A54.9) Gonococcal infection, unspecified
• (A55.) Chlamydial lymphogranuloma (venereum)
• (A56.) Other sexually transmitted chlamydial diseases
○ (A56.0) Chlamydial infection of lower genitourinary tract
○ (A56.1) Chlamydial infection of pelviperitoneum and other genitourinary
organs
○ (A56.2) Chlamydial infection of genitourinary tract, unspecified
○ (A56.3) Chlamydial infection of anus and rectum
○ (A56.4) Chlamydial infection of pharynx
○ (A56.8) Sexually transmitted chlamydial infection of other sites
• (A57.) Chancroid
• (A58.) Granuloma inguinale
• (A59.) Trichomoniasis
○ (A59.0) Urogenital trichomoniasis
○ (A59.8) Trichomoniasis of other sites
○ (A59.9) Trichomoniasis, unspecified
• (A60.) Anogenital herpesviral (herpes simplex) infection
○ (A60.0) Herpesviral infection of genitalia and urogenital tract
○ (A60.1) Herpesviral infection of perianal skin and rectum
○ (A60.9) Anogenital herpesviral infection, unspecified
• (A63.) Other predominantly sexually transmitted diseases, not elsewhere
classified
○ (A63.0) Anogenital (venereal) warts
○ (A63.8) Other specified predominantly sexually transmitted diseases
• (A64.) Unspecified sexually transmitted disease
[edit] (A65-A69) Other spirochaetal diseases
• (A65.) Nonvenereal syphilis
○ Bejel
○ Endemic syphilis
○ Njovera
• (A66.) Yaws
 • (A67.) Pinta (carate)
• (A68.) Relapsing fevers
• (A69.) Other spirochaetal infections
○ (A69.0) Necrotizing ulcerative stomatitis
 Cancrum oris
 Fusospirochaetal gangrene
 Noma
 Stomatitis gangrenosa
○ (A69.1) Other Vincent's infections
 Trench mouth
○ (A69.2) Lyme disease
 Erythema chronicum migrans due to Borrelia burgdorferi
○ (A69.8) Other specified spirochaetal infections
○ (A69.9) Spirochaetal infection, unspecified
[edit] (A70-A74) Other diseases caused by chlamydiae
• (A70.) Chlamydia psittaci infection
○ Psittacosis
• (A71.) Trachoma
• (A74.) Other diseases caused by chlamydiae
[edit] (A75-A79) Rickettsioses
• (A75.) Typhus fever
○ (A75.0) Epidemic louse-borne typhus fever due to Rickettsia prowazekii
○ (A75.1) Recrudescent typhus (Brill's disease)
 Brill-Zinsser disease
○ (A75.2) Typhus fever due to Rickettsia typhi
○ (A75.3) Typhus fever due to Rickettsia tsutsugamushi
 Scrub typhus
○ (A75.9) Typhus fever, unspecified
• (A77.) Spotted fever (tick-borne rickettsioses)
○ (A77.0) Spotted fever due to Rickettsia rickettsii
 Rocky Mountain spotted fever
 Sao Paulo fever
○ (A77.1) Spotted fever due to Rickettsia conorii
 African tick typhus
 Boutonneuse fever
 India tick typhus
 Kenya tick typhus
  Marseilles fever
 Mediterranean tick fever
○ (A77.2) Spotted fever due to Rickettsia sibirica
 North Asian tick fever
 Siberian tick typhus
○ (A77.3) Spotted fever due to Rickettsia australis
 Queensland tick typhus
○ (A77.8) Other spotted fevers
○ (A77.9) Spotted fever, unspecified
 Tick-borne typhus NOS
• (A78.) Q fever
• (A79.) Other rickettsioses
○ (A79.0) Trench fever
 Quintan fever
 Wolhynian fever
○ (A79.1) Rickettsialpox due to Rickettsia akari
 Kew Garden fever
 Vesicular rickettsiosis
○ (A79.8) Other specified rickettsioses
 Rickettsiosis due to Ehrlichia sennetsu
○ (A79.9) Rickettsiosis, unspecified
 Rickettsial infection NOS
[edit] A80-B34 - Viral infections
[edit] (A80-A89) Viral infections of the central nervous system
• (A80.) Acute poliomyelitis
• (A81.) Atypical virus infections of central nervous system
○ (A81.0) Creutzfeldt-Jakob disease
○ (A81.1) Subacute sclerosing panencephalitis
○ (A81.2) Progressive multifocal leukoencephalopathy
○ (A81.8) Other atypical virus infections of central nervous system
 Kuru
○ (A81.9) Atypical virus infection of central nervous system, unspecified
 Prion disease of central nervous system NOS
• (A82.) Rabies
• (A83.) Mosquito-borne viral encephalitis
○ (A83.0) Japanese encephalitis
○ (A83.1) Western equine encephalitis
 ○ (A83.2) Eastern equine encephalitis
○ (A83.3) St Louis encephalitis
○ (A83.4) Australian encephalitis
 Kunjin virus disease
○ (A83.5) California encephalitis
 California meningoencephalitis
 La Crosse encephalitis
○ (A83.6) Rocio virus disease
○ (A83.8) Other mosquito-borne viral encephalitis
○ (A83.9) Mosquito-borne viral encephalitis, unspecified
• (A84.) Tick-borne viral encephalitis
○ (A84.0) Far Eastern tick-borne encephalitis (Russian spring-summer
encephalitis)
○ (A84.1) Central European tick-borne encephalitis
○ (A84.8) Other tick-borne viral encephalitis
 Louping ill
 Powassan virus disease
○ (A84.9) Tick-borne viral encephalitis, unspecified
• (A85.) Other viral encephalitis, not elsewhere classified
○ (A85.8) Other specified viral encephalitis
 Encephalitis lethargica
• (A86.) Unspecified viral encephalitis
• (A87.) Viral meningitis
○ (A87.2) Lymphocytic choriomeningitis
• (A88.) Other viral infections of central nervous system, not elsewhere classified
○ (A88.1) Epidemic vertigo
• (A89.) Unspecified viral infection of central nervous system
[edit] (A90-A99) Arthropod-borne viral fevers and viral haemorrhagic
fevers
• (A90.) Dengue fever (classical dengue)
• (A91.) Dengue haemorrhagic fever
• (A92.) Other mosquito-borne viral fevers
○ (A92.0) Chikungunya virus disease
○ (A92.1) O'nyong-nyong fever
○ (A92.2) Venezuelan equine fever
○ (A92.3) West Nile virus infection
○ (A92.4) Rift Valley fever
○ (A92.8) Other specified mosquito-borne viral fevers
 ○ (A92.9) Mosquito-borne viral fever, unspecified
• (A93.) Other arthropod-borne viral fevers, not elsewhere classified
○ (A93.0) Oropouche virus disease
 Oropouche fever
○ (A93.1) Sandfly fever
 Pappataci fever
 Phlebotomus fever
○ (A93.2) Colorado tick fever
○ (A93.8) Other specified arthropod-borne viral fevers
 Piry virus disease
 Vesicular stomatitis virus disease (Indiana fever)
• (A94.) Unspecified arthropod-borne viral fever
• (A95.) Yellow fever
• (A96.) Arenaviral haemorrhagic fever
○ (A96.0) Argentine hemorrhagic fever (Junín virus)
○ (A96.1) Machupo haemorrhagic fever
 Bolivian hemorrhagic fever
○ (A96.2) Lassa fever
• (A98.) Other viral haemorrhagic fevers, not elsewhere classified
○ (A98.0) Crimean-Congo haemorrhagic fever
○ (A98.1) Omsk haemorrhagic fever
○ (A98.2) Kyasanur Forest disease
○ (A98.3) Marburg virus disease
○ (A98.4) Ebola virus disease
○ (A98.5) Haemorrhagic fever with renal syndrome
• (A99.) Unspecified viral haemorrhagic fever
[edit] (B00-B09) Viral infections characterized by skin and mucous
membrane lesions
• (B00.) Herpesviral (herpes simplex) infections
○ (B00.0) Eczema herpeticum
○ (B00.1) Herpesviral vesicular dermatitis
○ (B00.2) Herpesviral gingivostomatitis and pharyngotonsillitis
○ (B00.3) Herpesviral meningitis
○ (B00.4) Herpesviral encephalitis
○ (B00.5) Herpesviral ocular disease
○ (B00.7) Disseminated herpesviral disease
○ (B00.8) Other forms of herpesviral infection
 ○ (B00.9) Herpesviral infection, unspecified
• (B01.) Varicella (chickenpox)
○ (B01.0) Varicella meningitis
○ (B01.1) Varicella encephalitis
○ (B01.2) Varicella pneumonia
○ (B01.8) Varicella with other complications
○ (B01.9) Varicella without complication
• (B02.) Zoster (herpes zoster)
○ (B02.0) Zoster encephalitis
○ (B02.1) Zoster meningitis
○ (B02.2) Zoster with other nervous system involvement
○ (B02.3) Zoster ocular disease
○ (B02.7) Disseminated zoster
○ (B02.8) Zoster with other complications
○ (B02.9) Zoster without complication
• (B03.) Smallpox
• (B04.) Monkeypox
• (B05.) Measles
• (B06.) Rubella (German measles)
• (B07.) Viral warts
○ Verruca
• (B08.) Other viral infections characterized by skin and mucous membrane
lesions, not elsewhere classified
○ (B08.0) Other orthopoxvirus infections
 Cowpox
 Orf virus disease
 Pseudocowpox
 Vaccinia
○ (B08.1) Molluscum contagiosum
○ (B08.2) Exanthema subitum (sixth disease)
○ (B08.3) Erythema infectiosum (fifth disease)
○ (B08.4) Enteroviral vesicular stomatitis with exanthem
 Hand, foot and mouth disease
○ (B08.5) Enteroviral vesicular pharyngitis
 Herpangina
○ (B08.8) Other specified viral infections characterized by skin and mucous
membrane lesions
 Enteroviral lymphonodular pharyngitis
  Foot-and-mouth disease
 Tanapox virus disease
 Yaba pox virus disease
• (B09.) Unspecified viral infection characterized by skin and mucous membrane
lesions
○ Viral enanthema NOS
○ Viral exanthema NOS
[edit] (B15-B19) Viral hepatitis
• (B15.) Acute hepatitis A
• (B16.) Acute hepatitis B
• (B17.) Other acute viral hepatitis
○ (B17.0) Acute delta-(super)infection of hepatitis B carrier
○ (B17.1) Acute hepatitis C
○ (B17.2) Acute hepatitis E
• (B18.) Chronic viral hepatitis
• (B19.) Unspecified viral hepatitis
[edit] (B20-B24) Human immunodeficiency virus (HIV) disease
• (B20.) Human Immunodeficiency Virus (HIV) disease Resulting in infectious
and parasitic diseases
○ (B20.0) HIV disease resulting in mycobacterial infection
○ (B20.1) HIV disease resulting in other bacterial infections
○ (B20.2) HIV disease resulting in cytomegaloviral disease
○ (B20.3) HIV disease resulting in other viral infections
○ (B20.4) HIV disease resulting in candidiasis
○ (B20.5) HIV disease resulting in other mycoses
○ (B20.6) HIV disease resulting in Pneumocystis pneumonia
○ (B20.7) HIV disease resulting in multiple infections
○ (B20.8) HIV disease resulting in other infectious and parasitic diseases
○ (B20.9) HIV disease resulting in unspecified infectious or parasitic
disease
• (B21.) Human Immunodeficiency Virus (HIV) disease Resulting in malignant
neoplasms
○ (B21.0) HIV disease resulting in Kaposi's sarcoma
○ (B21.1) HIV disease resulting in Burkitt's lymphoma
○ (B21.2) HIV disease resulting in other types of non-Hodgkin's lymphoma
○ (B21.3) HIV disease resulting in other malignant neoplasms of lymphoid,
haematopoietic and related tissue
○ (B21.7) HIV disease resulting in multiple malignant neoplasms
 ○ (B21.8) HIV disease resulting in other malignant neoplasms
○ (B21.9) HIV disease resulting in unspecified malignant neoplasm
• (B22.) Human Immunodeficiency Virus (HIV) disease Resulting in other
specified diseases
○ (B22.0) HIV disease resulting in encephalopathy
○ (B22.1) HIV disease resulting in lymphoid interstitial pneumonitis
○ (B22.2) HIV disease resulting in wasting syndrome
○ (B22.7) HIV disease resulting in multiple diseases classified elsewhere
• (B23.) Human Immunodeficiency Virus (HIV) disease Resulting in other
conditions
○ (B23.0) Acute HIV infection syndrome
○ (B23.1) HIV disease resulting in (persistent) generalized
lymphadenopathy
○ (B23.2) HIV disease resulting in haematological and immunological
abnormalities, not elsewhere classified
○ (B23.8) HIV disease resulting in other specified conditions
• (B24.) Unspecified Human Immunodeficiency Virus (HIV) Disease
[edit] (B25-B34) Other viral diseases
• (B25.) Cytomegaloviral disease
• (B26.) Mumps
• (B27.) Infectious mononucleosis
• (B30.) Viral conjunctivitis
• (B33.) Other viral diseases, not elsewhere classified
○ (B33.0) Epidemic myalgia
 Bornholm disease
○ (B33.1) Ross River disease
 Epidemic polyarthritis and exanthema
 Ross River fever
○ (B33.2) Viral carditis
○ (B33.3) Retrovirus infections, not elsewhere classified
○ (B33.4) Hantavirus (cardio-)pulmonary syndrome (HPS) (HCPS)
○ (B33.9) Other specified viral diseases
• (B34.) Viral infection of unspecified site
[edit] B35-B89 - Infections caused by fungi, protozoans,
worms, and infestations
[edit] (B35-B49) Mycoses
• (B35.) Dermatophytosis
○ (B35.0) Tinea barbae and tinea capitis
  Beard Ringworm
 Kerion
 Tinea capitis
 Sycosis, mycotic
○ (B35.1) Tinea unguium
 Dermatophytic onychia
 Dermatophytosis of nail
 Onychomycosis
 Ringworm of nails
○ (B35.2) Tinea manuum
○ (B35.3) Tinea pedis
○ (B35.4) Tinea corporis
○ (B35.5) Tinea imbricata
○ (B35.6) Tinea cruris
• (B36.) Other superficial mycoses
○ (B36.0) Pityriasis versicolor
○ (B36.1) Tinea nigra
○ (B36.2) White piedra
○ (B36.3) Black piedra
○ (B36.8) Other specified superficial mycoses
○ (B36.9) Superficial mycosis, unspecified
• (B37.) Candidiasis
○ (B37.0) Candidal stomatitis
 Oral thrush
○ (B37.1) Pulmonary candidiasis
○ (B37.2) Candidiasis of skin and nail
○ (B37.3) Candidiasis of vulva and vagina
○ (B37.4) Candidiasis of other urogenital sites
○ (B37.5) Candidal meningitis
○ (B37.6) Candidal endocarditis
○ (B37.7) Candidal septicaemia
○ (B37.8) Candidiasis of other sites
○ (B37.9) Candidiasis, unspecified
• Dimorphic Fungi
○ (B38.) Coccidioidomycosis
○ (B39.) Histoplasmosis
○ (B40.) Blastomycosis
 ○ (B41.) Paracoccidioidomycosis
○ (B42.) Sporotrichosis
• (B43.) Chromomycosis and phaeomycotic abscess
• (B44.) Aspergillosis
• (B45.) Cryptococcosis
• (B46.) Zygomycosis
○ (B46.0) Pulmonary mucormycosis
○ (B46.1) Rhinocerebral mucormycosis
○ (B46.2) Gastrointestinal mucormycosis
○ (B46.3) Cutaneous mucormycosis
○ (B46.4) Disseminated mucormycosis
○ (B46.5) Mucormycosis, unspecified
○ (B46.8) Other zygomycoses
 Entomophthoromycosis
○ (B46.9) Zygomycosis, unspecified
• (B47.) Mycetoma
○ (B47.0) Eumycetoma
 Madura Foot, mycotic
 Maduromycosis
○ (B47.1) Actinomycetoma
○ (B47.9) Mycetoma, unspecified
 Madura Foot NOS
• (B48.) Other mycoses, not elsewhere classified
○ (B48.0) Lobomycosis
 Keloidal blastomycosis
 Lobo's disease
○ (B48.1) Rhinosporidiosis
○ (B48.2) Allescheriasis
 Infection due to Pseudallescheria boydii
○ (B48.3) Geotrichosis
 Geotrichum stomatitis
○ (B48.4) Penicillosis
○ (B48.7) Opportunistic mycoses
○ (B48.8) Other specified mycoses
 Adiaspiromycosis
• (B49.) Unspecified mycosis
[edit] (B50-B64) Protozoal diseases
 • (B50.) Plasmodium falciparum malaria
• (B51.) Plasmodium vivax malaria
• (B52.) Plasmodium malariae malaria
• (B53.) Other parasitologically confirmed malaria
• (B54.) Unspecified malaria
• (B55.) Leishmaniasis
○ (B55.0) Visceral leishmaniasis
○ (B55.1) Cutaneous leishmaniasis
○ (B55.2) Mucocutaneous leishmaniasis
○ (B55.9) Leishmaniasis, unspecified
• (B56.) African trypanosomiasis
• (B57.) Chagas' disease
• (B58.) Toxoplasmosis
• (B59.) Pneumocystosis
• (B60.) Other protozoal diseases, not elsewhere classified
○ (B60.0) Babesiosis
 Piroplasmosis
○ (B60.1) Acanthamoebiasis
○ (B60.2) Naegleriasis
 Primary amoebic meningoencephalitis
○ (B60.8) Other specified protozoal diseases
 Microsporidiosis
• (B64.) Unspecified protozoal disease
[edit] (B65-B83) Helminthiases
• (B65.) Schistosomiasis (bilharziasis)
○ (B65.0) Schistosomiasis due to Schistosoma haematobium (urinary
schistosomiasis)
○ (B65.1) Schistosomiasis due to Schistosoma mansoni (intestinal
schistosomiasis)
○ (B65.2) Schistosomiasis due to Schistosoma japonicum
○ (B65.3) Cercarial dermatitis
○ (B65.8) Other schistosomiases
○ (B65.9) Schistosomiasis, unspecified
• (B66.) Other fluke infections
○ (B66.0) Opisthorchiasis
○ (B66.1) Clonorchiasis
○ (B66.2) Dicrocoeliasis
○ (B66.3) Fascioliasis
 ○ (B66.4) Paragonimiasis
○ (B66.5) Fasciolopsiasis
○ (B66.8) Other specified fluke infections
• (B67.) Echinococcosis
• (B68.) Taeniasis
○ (B68.0) Taenia solium taeniasis
 Pork tapeworm
○ (B68.1) Taenia saginata taeniasis
 Beef tapeworm
• (B69.) Cysticercosis
• (B70.) Diphyllobothriasis and sparganosis
○ (B70.0) Diphyllobothriasis
○ (B70.1) Sparganosis
• (B71.) Other cestode infections
○ (B71.0) Hymenolepiasis
 Dwarf tapeworm
• (B72.) Dracunculiasis
• (B73.) Onchocerciasis
• (B74.) Filariasis
○ (B74.0) Filariasis due to Wuchereria bancrofti
 Elephantiasis, filarial (ILDS B74.01)
○ (B74.1) Filariasis due to Brugia malayi
○ (B74.2) Filariasis due to Brugia timori
○ (B74.3) Loiasis
○ (B74.4) Mansonelliasis
○ (B74.8) Other filariases
○ (B74.9) Filariasis, unspecified
• (B75.) Trichinellosis
• (B76.) Hookworm diseases
○ (B76.0) Ancylostomiasis
○ (B76.1) Necatoriasis
○ (B76.8) Other hookworm diseases
○ (B76.9) Hookworm disease, unspecified
 Cutaneous larva migrans NOS
• (B77.) Ascariasis
• (B78.) Strongyloidiasis
• (B79.) Trichuriasis
 • (B80.) Enterobiasis
• (B81.) Other intestinal helminthiases, not elsewhere classified
○ (B81.0) Anisakiasis
○ (B81.1) Intestinal capillariasis
○ (B81.2) Trichostrongyliasis
○ (B81.3) Intestinal angiostrongyliasis
○ (B81.4) Mixed intestinal helminthiases
○ (B81.8) Other specified intestinal helminthiases
• (B82.) Unspecified intestinal parasitism
• (B83.) Other helminthiases
○ (B83.0) Visceral larva migrans
○ (B83.1) Gnathostomiasis
○ (B83.2) Angiostrongyliasis due to Parastrongylus cantonensis
○ (B83.3) Syngamiasis
○ (B83.4) Internal hirudiniasis
○ (B83.8) Other specified helminthiases
 Acanthocephaliasis
 Gongylonemiasis
 Hepatic capillariasis
 Metastrongyliasis
 Thelaziasis
○ (B83.9) Helminthiasis, unspecified
[edit] (B85-B89) Pediculosis, acariasis and other infestations
• (B85.) Pediculosis and phthiriasis
○ (B85.0) Pediculosis due to Pediculus humanus capitis
○ (B85.1) Pediculosis due to Pediculus humanus corporis
○ (B85.2) Pediculosis, unspecified
○ (B85.3) Phthiriasis
○ (B85.4) Mixed pediculosis and phthiriasis
• (B86.) Scabies
• (B87.) Myiasis
• (B88.) Other infestations
○ (B88.0) Other acariasis
 Acarine dermatitis
 Dermatitis due to Demodex species
 Dermatitis due to Dermanyssus gallinae
 Dermatitis due to Liponyssoides sanguineus
  Trombiculosis
○ (B88.1) Tungiasis (sandflea infestation)
○ (B88.2) Other arthropod infestations
 Scarabiasis
○ (B88.3) External hirudiniasis
 Leech infestation NOS
○ (B88.8) Other specified infestations
 Ichthyoparasitism due to Vandellia cirrhosa
 Linguatulosis
 Porocephaliasis
○ (B88.9) Infestation, unspecified
 Infestation (skin) NOS
 Infestation by mites NOS
 Skin parasites NOS
• (B89.) Unspecified parasitic disease
[edit] B90-B99 - Sequelae, and diseases classified
elsewhere
[edit] (B90-B94) Sequelae of infectious and parasitic diseases
• (B90.) Sequelae of tuberculosis
• (B91.) Sequelae of poliomyelitis
• (B92.) Sequelae of leprosy
• (B94.) Sequelae of other and unspecified infectious and parasitic diseases
○ (B94.0) Sequelae of trachoma
○ (B94.1) Sequelae of viral encephalitis
○ (B94.2) Sequelae of viral hepatitis
○ (B94.8) Sequelae of other specified infectious and parasitic diseases
○ (B94.9) Sequelae of unspecified infectious or parasitic disease
[edit] (B95-B97) Bacterial, viral and other infectious agents
• (B95.) Streptococcus and staphylococcus as the cause of diseases classified to
other chapters
○ (B95.0) Streptococcus, group A, as the cause of diseases classified to
other chapters
○ (B95.1) Streptococcus, group B, as the cause of diseases classified to
other chapters
○ (B95.2) Streptococcus, group D, as the cause of diseases classified to
other chapters
○ (B95.3) Streptococcus pneumoniae as the cause of diseases classified to
other chapters
 ○ (B95.4) Other streptococcus as the cause of diseases classified to other
chapters
○ (B95.5) Unspecified streptococcus as the cause of diseases classified to
other chapters
○ (B95.6) Staphylococcus aureus as the cause of diseases classified to other
chapters
○ (B95.7) Other staphylococcus as the cause of diseases classified to other
chapters
○ (B95.8) Unspecified staphylococcus as the cause of diseases classified to
other chapters
• (B96.) Other bacterial agents as the cause of diseases classified to other chapters
○ (B96.0) Mycoplasma pneumoniae (M. pneumoniae) as the cause of
diseases classified to other chapters
○ (B96.1) Klebsiella pneumoniae (K. pneumoniae) as the cause of diseases
classified to other chapters
○ (B96.2) Escherichia coli (E. coli) as the cause of diseases classified to
other chapters
○ (B96.3) Haemophilus influenzae (H. influenzae) as the cause of diseases
classified to other chapters
○ (B96.4) Proteus (mirabilis)(morganii) as the cause of diseases classified to
other chapters
○ (B96.5) Pseudomonas (aeruginosa)(mallei)(pseudomallei) as the cause of
diseases classified to other chapters
○ (B96.6) Bacillus fragilis (B. fragilis) as the cause of diseases classified to
other chapters
○ (B96.7) Clostridium perfringens (C. perfringens) as the cause of diseases
classified to other chapters
○ (B96.8) Other specified bacterial agents as the cause of diseases classified
to other chapters
• (B97.) Viral agents as the cause of diseases classified to other chapters
○ (B97.0) Adenovirus as the cause of diseases classified to other chapters
○ (B97.1) Enterovirus as the cause of diseases classified to other chapters
 Coxsackievirus
 Echovirus
○ (B97.2) Coronavirus as the cause of diseases classified to other chapters
○ (B97.3) Retrovirus as the cause of diseases classified to other chapters
 Lentivirus
 Oncovirus
○ (B97.4) Respiratory syncytial virus as the cause of diseases classified to
other chapters
○ (B97.5) Reovirus as the cause of diseases classified to other chapters
 ○ (B97.6) Parvovirus as the cause of diseases classified to other chapters
○ (B97.7) Papillomavirus as the cause of diseases classified to other
chapters
○ (B97.8) Other viral agents as the cause of diseases classified to other
chapters
[edit] (B99) Other infectious diseases
• (B99.) Other and unspecified infectious diseases
[edit] See also
• International Statistical Classification of Diseases and Related Health Problems
• List of ICD-10 codes
[edit] References
1. ^ WHO | International Classification of Diseases (ICD)
[show]
v•d•e
Pathology: Medical conditions and ICD code

(Disease / Disorder / Illness, Syndrome / Sequence, Symptom / Sign, Injury, etc.)

(
A
/
B
,

0Infectious disease/Infection: Bacterial disease (G+, G-) · Virus disease · Parasitic disease
0(Protozoan infection, Helminthiasis, Ectoparasitic infestation) · Mycosis · Zoonosis
1
-
1
3
9
)

(Cancer
C(C00-D48, Tumor
/140-239)
D
,Myeloid
hematologic
1(D50-D77, Anemia · Coagulopathy
4280-289)
0
-Lymphoid
2immune
3(D80-D89, Immunodeficiency · Immunoproliferative disorder · Hypersensitivity
9279)
&

2
7
9
-
2
8
9
)

(
E
,

2
4
Endocrine disease · Nutrition disorder · Inborn error of metabolism
0
-
2
7
8
)

(
F
,

2
9
Mental disorder
0
-
3
1
9
)

(
G
,

3
2
Nervous system disease (CNS, PNS) · Neuromuscular disease
0
-
3
5
9
)

(Eye disease · Ear disease

H
,

3
6
0
-
3
8
9
)

(
I
,

3
9
Cardiovascular disease (Heart disease, Vascular disease)
0
-
4
5
9
)

(
J
,

4
6
Respiratory disease (Obstructive lung disease, Restrictive lung disease, Pneumonia)
0
-
5
1
9
)

(
K
,

5
2Stomatognathic disease (Tooth disease) · Digestive disease (Esophageal, Stomach,
0Enteropathy, Liver, Pancreatic)
-
5
7
9
)
(
L
,

6
8
Skin disease · skin appendages (Nail disease, Hair disease, Sweat gland disease)
0
-
7
0
9
)

(
M
,

7
1Musculoskeletal disorders: Myopathy · Arthropathy · Osteochondropathy (Osteopathy,
0Chondropathy)
-
7
3
9
)

(
N
,

5
8Urologic disease (Nephropathy, Urinary bladder disease) · Male genital disease · Breast
0disease · Female genital disease
-
6
2
9
)

(
O
,

6
3
Complications of pregnancy · Obstetric labor complication · Puerperal disorder
0
-
6
7
9
)
(
P
,

7
6
Fetal disease
0
-
7
7
9
)

(
Q
,

7
4
Congenital disorder (Congenital abnormality)
0
-
7
5
9
)

(
R
,

7
8
Syndromes · Medical signs (Eponymous)
0
-
7
9
9
)

(Bone fracture · Joint dislocation · Sprain · Strain · Subluxation · Head injury · Chest
Strauma · Poisoning
/
T
,

8
0
0
-
9
9
9
)

[show]
v•d•e
Sexually transmitted diseases and infections (STD/STI) (primarily A50–A64,
090–099)

B
a
c
Chancroid (Haemophilus ducreyi) · Chlamydia/Lymphogranuloma
t
venereum (Chlamydia trachomatis) · Donovanosis or Granuloma Inguinale (Klebsiella
e
granulomatis) · Gonorrhea (Neisseria gonorrhoeae) · Syphilis (Treponema pallidum) ·
r
Ureaplasma infection (Ureaplasma urealyticum)
i
a
l

P
r
o
t
oTrichomoniasis (Trichomonas vaginalis)
z
o
a
l

P
a
r
a
sCrab louse/crabs · Scabies
i
t
i
c

V
iAIDS (HIV-1/HIV-2) · Cervical cancer & Genital warts (condyloma) (Human
rpapillomavirus (HPV)) · Hepatitis B (Hepatitis B virus) · Herpes simplex (HSV1/HSV2) ·
aMolluscum contagiosum (MCV)
l

G
efemale: Cervicitis · Pelvic inflammatory disease (PID)
n
emale: Epididymitis · Prostatitis
reither: Proctitis · Urethritis/Non-gonococcal urethritis (NGU)
a
l

i
n
f
l
a
m
m
a
t
i
o
n

M: ♀ FRS anat/phys/devp noco/cong/npls, proc/asst, drug

sysi/epon (G1/G2B/G3CD)

M: ♂ MRS anat/phys/devp noco/cong/tumr, proc, drug

sysi/epon (G3B/4B/4C)

[show]
v•d•e
Firmicutes (low-G+C) Infectious diseases · Bacterial diseases: G+ (primarily
A00–A79, 001–041, 080–109)

B optochin susceptible: S. pneumoniae (Pneumococcal

a infection)
c α
optochin resistant: S. viridans (S. mitis, S. mutans, S.
i oralis, S. sanguinis, S. sobrinus, milleri group)
l
l Streptococcus
iLactobacillales A, bacitracin susceptible: S. pyogenes (Scarlet fever,
βErysipelas, Rheumatic fever, Streptococcal pharyngitis)
(Cat-)
B, bacitracin resistant, CAMP test+: S. agalactiae

γD, BEA+: Streptococcus bovis

BEA+: Enterococcus faecalis (Urinary tract infection) ·

Enterococcus
Enterococcus faecium

Bacillales Cg+ S. aureus (Staphylococcal scalded skin syndrome,

(Cat+) Toxic shock syndrome, MRSA)
Staphylococcus
Cg- novobiocin susceptible (S. epidermidis) · novobiocin
resistant (S. saprophyticus)

Bacillus anthracis (Anthrax) · Bacillus cereus (Food

Bacillus
poisoning)
 Listeria Listeria monocytogenes (Listeriosis)

C motile: Clostridium difficile (Pseudomembranous colitis) ·

lClostridium Clostridium botulinum (Botulism) · Clostridium tetani (Tetanus)
o(spore-forming)
s nonmotile: Clostridium perfringens (Gas gangrene, Clostridial
t necrotizing enteritis)
r
iPeptostreptococcus
d(non-spore Peptostreptococcus magnus
iforming)
a

M Ureaplasma urealyticum (Ureaplasma infection) · Mycoplasma

oMycoplasmataceae
genitalium · Mycoplasma pneumoniae (Mycoplasma pneumonia)
l
lAnaeroplasmatales Erysipelothrix rhusiopathiae (Erysipeloid)
i
c
u
t
e
s

M: BAC bact (clas) gr+f/gr+a(t)/gr-p(c)/gr- drug(J1p, w, n, m,

o vacc)

[show]
v•d•e
Actinobacteria (high-G+C) Infectious diseases · Bacterial diseases: G+
(primarily A00–A79, 001–041, 080–109)

A Actinomyces israelii (Actinomycosis, Cutaneous actinomycosis) ·

cActinomycetaceae Tropheryma whipplei (Whipple's disease) · Arcanobacterium
t haemolyticum (Arcanobacterium haemolyticum infection)
i
nPropionibacteriaceaePropionibacterium acnes
o
m
y
c
i
n
e
a
e

C
Mycobacteriaceae M. Tuberculosis: Ghon focus/Ghon's complex · Pott
o tuberculosis/ disease · brain (Meningitis, Rich focus) ·
r M. bovis Tuberculous lymphadenitis (Tuberculous cervical
 lymphadenitis) · cutaneous (Scrofuloderma,
Erythema induratum, Lupus vulgaris, Prosector's
wart, Tuberculosis cutis orificialis, Tuberculous
cellulitis, Tuberculous gumma) · Lichen
scrofulosorum · Tuberculid (Papulonecrotic
tuberculid) · Primary inoculation tuberculosis ·
Miliary · Tuberculous pericarditis · Urogenital
tuberculosis · Multi-drug-resistant tuberculosis ·
Extensively drug-resistant tuberculosis
y
n Leprosy: Tuberculoid leprosy · Borderline
e tuberculoid leprosy · Borderline leprosy · Borderline
b M. leprae
lepromatous leprosy · Lepromatous leprosy · Histoid
a leprosy
c
t
e R1: M. kansasii · M. marinum (Aquarium
r granuloma)
i R2: M. gordonae
n
Nontuberculous R3: M. avium complex/Mycobacterium
e avium/Mycobacterium intracellulare/MAP (MAI
a infection) · M. ulcerans (Buruli ulcer) · M.
e haemophilum
R4/RG: M. fortuitum · M. chelonae · M. abscessus

Nocardia asteroides/Nocardia brasiliensis (Nocardiosis) ·

Nocardiaceae
Rhodococcus equi

Corynebacterium diphtheriae (Diphtheria) · Corynebacterium

Corynebacteriaceae minutissimum (Erythrasma) · Corynebacterium jeikeium (Group JK
corynebacterium sepsis)

B
i
f
i
d
o
b
a
c
Gardnerella vaginalis
t
e
r
i
a
c
e
a
e
 M: BAC bact (clas) gr+f/gr+a(t)/gr-p(c)/gr- drug(J1p, w, n, m,
o vacc)

[show]
v•d•e
Infectious diseases · Bacterial diseases: Proteobacterial G- (primarily A00–
A79, 001–041, 080–109)

Rickettsia typhi (Murine typhus) · Rickettsia

Typhus prowazekii (Epidemic typhus, Brill–Zinsser
disease, Flying squirrel typhus)

Rickettsia rickettsii (Rocky Mountain

spotted fever) · Rickettsia conorii
(Boutonneuse fever) · Rickettsia japonica
(Japanese spotted fever) · Rickettsia sibirica
(North Asian tick typhus) · Rickettsia
Tick-
australis (Queensland tick typhus) ·
Rickettsiaceae/ borne
Rickettsia honei (Flinders Island spotted
(Rickettsioses)
fever) · Rickettsia africae (African tick bite
Spotted fever) · Rickettsia parkeri (American tick
Rickettsiales fever bite fever) · Rickettsia aeschlimannii
(Rickettsia aeschlimannii infection)

α Mite- Rickettsia akari (Rickettsialpox) · Orientia

borne tsutsugamushi (Scrub typhus)

Flea-
Rickettsia felis (Flea-borne spotted fever)
borne

Ehrlichiosis: Anaplasma phagocytophilum (Human

granulocytic anaplasmosis, Anaplasmosis) · Ehrlichia
Anaplasmataceae
chaffeensis (Human monocytic ehrlichiosis) · Ehrlichia
ewingii (Ehrlichiosis ewingii infection)

Brucellaceae Brucella abortus (Brucellosis)

Bartonellosis: Bartonella henselae (Cat scratch disease) ·

Rhizobiales
Bartonella quintana (Trench fever) · either henselae or
Bartonellaceae
quintana (Bacillary angiomatosis) · Bartonella bacilliformis
(Carrion's disease, Verruga peruana)

β M+ Neisseria meningitidis/meningococcus (Meningococcal disease,

Waterhouse-Friderichsen syndrome, Meningococcal septicaemia)
Neisseriales M- Neisseria gonorrhoeae/gonococcus (Gonorrhea)
ungrouped: Eikenella corrodens/Kingella kingae (HACEK) ·
Chromobacterium violaceum (Chromobacteriosis infection)

BurkholderialesBurkholderia pseudomallei (Melioidosis) · Burkholderia mallei

 (Glanders) · Burkholderia cepacia complex · Bordetella
pertussis/Bordetella parapertussis (Pertussis)

Klebsiella pneumoniae (Rhinoscleroma, Klebsiella

pneumonia) · Klebsiella granulomatis (Granuloma
inguinale) · Klebsiella oxytoca
Lac+ Escherichia coli: Enterotoxigenic · Enteroinvasive ·
O157:H7/Enterohemorrhagic (Hemolytic-uremic
syndrome)
Enterobacter aerogenes/Enterobacter cloacae

Enterobacteriales Serratia marcescens (Serratia infection) · Citrobacter

Slow/weak
(OX-) koseri/Citrobacter freundii

Salmonella enterica (Typhoid fever, Paratyphoid

H2S+
fever, Salmonellosis)

Shigella dysenteriae/sonnei/flexneri/boydii
Lac-
(Shigellosis, Bacillary dysentery) · Proteus
H2S- mirabilis/Proteus vulgaris · Yersinia pestis
(Plague/Bubonic plague) · Yersinia enterocolitica ·
Yersinia pseudotuberculosis

γ Haemophilus: H. influenzae (Haemophilus meningitis, Brazilian

purpuric fever) · H. ducreyi (Chancroid) H. parainfluenzae (HACEK)
Pasteurellales Pasteurella multocida (Pasteurellosis) · Actinobacillus
(Actinobacillosis)
Aggregatibacter actinomycetemcomitans (HACEK)

Legionella pneumophila/Legionella longbeachae (Legionellosis) ·

Legionellales
Coxiella burnetii (Q fever)

Thiotrichales Francisella tularensis (Tularemia)

Vibrio cholerae (Cholera) · Vibrio vulnificus · Vibrio

Vibrionales
parahaemolyticus · Vibrio alginolyticus · Plesiomonas shigelloides

Pseudomonas aeruginosa (Pseudomonas infection) · Moraxella

Pseudomonadales
catarrhalis · Acinetobacter baumannii

XanthomonadalesStenotrophomonas maltophilia

Cardiobacteriales Cardiobacterium hominis (HACEK)

Aeromonadales Aeromonas hydrophila/Aeromonas veronii (Aeromonas infection)

εCampylobacteralesCampylobacter jejuni (Campylobacteriosis, Guillain-Barré

syndrome) · Helicobacter pylori (Peptic ulcer, MALT lymphoma) ·
 Helicobacter cinaedi (Helicobacter cellulitis)

M: BAC bact (clas) gr+f/gr+a(t)/gr-p(c)/gr- drug(J1p, w, n, m,

o vacc)

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v•d•e
Infectious diseases · Bacterial diseases: BV4 non-proteobacterial G-
(primarily A00-A79, 001-041,080-109)

Treponema pallidum (Syphilis/Bejel, Yaws) · Treponema

Treponema
S carateum (Pinta) · Treponema denticola
p
i Borrelia burgdorferi/Borrelia afzelii (Lyme disease,
rSpirochaetaceae Erythema chronicum migrans, Neuroborreliosis)
o Borrelia Borrelia recurrentis (Louse borne relapsing fever) · Borrelia
c
h hermsii/Borrelia duttoni/Borrelia parkeri (Tick borne
a relapsing fever)
e
tLeptospiraceae LeptospiraLeptospira interrogans (Leptospirosis)
e
Spirillaceae SpirillumSpirillum minus (Rat-bite fever/Sodoku)

CChlamydophilaChlamydophila psittaci (Psittacosis) · Chlamydophila pneumoniae

h
l Chlamydia trachomatis (Chlamydia, Lymphogranuloma venereum,
aChlamydia Trachoma)
m
y
d
i
a
e

B
a
c
t
e
r
Bacteroides fragilis · Bacteroides forsythus · Capnocytophaga canimorsus ·
o
Porphyromonas gingivalis · Prevotella intermedia
i
d
e
t
e
s

FFusobacterium necrophorum (Lemierre's syndrome) · Fusobacterium nucleatum ·

u
s
o
b
a
Fusobacterium polymorphum
c
tStreptobacillus moniliformis (Rat-bite fever/Haverhill fever)
e
r
i
a

M: BAC bact (clas) gr+f/gr+a(t)/gr-p(c)/gr- drug(J1p, w, n, m,

o vacc)

[show]
v•d•e
Infectious diseases · Viral systemic diseases (A80–B34, 042–079)

O
n
DNA virus: HBV (Hepatocellular carcinoma) · HPV (Cervical cancer, Anal cancer) ·
c
Kaposi's sarcoma-associated herpesvirus (Kaposi's sarcoma) · Epstein-Barr virus
o
(Nasopharyngeal carcinoma, Burkitt's lymphoma, Primary central nervous system
v
lymphoma) · MCPyV (Merkel cell cancer) · SV40
i
rRNA virus: HCV (Hepatocellular carcinoma) · HTLV-I (Adult T-cell
uleukemia/lymphoma)
s

I
m
m
u
n
e

d
HIV (AIDS)
i
s
o
r
d
e
r
s

CEncephalitis/ DNA virus: JCV

emeningitis (Progressive
n multifocal
t leukoencephalopathy)
r
 RNA virus: MeV
(Subacute sclerosing
panencephalitis) ·
LCV (Lymphocytic
choriomeningitis) ·
a Arbovirus
l encephalitis ·
Orthomyxoviridae
n (probable)
e (Encephalitis
r lethargica) · RV
v (Rabies) · Chandipura
o virus · Herpesviral
u meningitis · Ramsay
s Hunt syndrome type
II
s
y Poliovirus
s (Poliomyelitis, Post-
tMyelitis polio syndrome) ·
e HTLV-I (Tropical
m spastic paraparesis)

Cytomegalovirus
(Cytomegalovirus
Eye
retinitis) · HSV
(Herpetic keratitis)

C
a
r
d
i
o
v
CBV (Pericarditis, Myocarditis)
a
s
c
u
l
a
r

R Epstein-Barr virus
e (EBV
sDNA virus infection/Infectious
p mononucleosis) ·
i Cytomegalovirus
r
aRNA virus
IV: SARS
t
coronavirus
o (Severe acute
r respiratory
y syndrome)
s V,
y Orthomyxoviridae:
s Influenzavirus
t A/B/C
e (Influenza/Avian
m influenza)
/ V, Paramyxovirus:
Human
a parainfluenza
c viruses
u (Parainfluenza) ·
t RSV · hMPV
e

v
i
r
a
l

n
a
s
o
p
h
a
r
y
n
g
i
t
i
s
/

v
i
r
a
l

p
n
e
u
m
o
n
i
a

MuV (Mumps) ·
Cytomegalovirus
Oropharynx/Esophagus
(Cytomegalovirus
esophagitis)
D
i DNA virus:
g Adenovirus
e (Adenovirus
s infection)
Gastroenteritis/
t RNA virus:
diarrhea
i Rotavirus ·
v Norovirus ·
e Astrovirus ·
Coronavirus
s
y DNA virus: HBV
s (B)
t RNA virus:
eHepatitis CBV · HAV (A) ·
m HCV (C) · HDV
(D) · HEV (E) ·
HGV (G)

Pancreatitis CBV

U
r
o
g
e
BK virus · MuV (Mumps)
n
i
t
a
l

M: VIR virs (prot) cutn/syst (hppv, hiva, drugJ(dnaa, rnaa, rtva,

infl, zost, zoon), epon vacc)

[show]
v•d•e
Zoonotic viral diseases (A80–B34, 042–079)

A
MosquitoBunyaviridae Arbovirus encephalitis: La Crosse encephalitis (LCV) · California
r
 encephalitis (CEV)
Viral hemorrhagic fever: Rift Valley fever (RVFV)

t Arbovirus encephalitis: Japanese encephalitis (JEV) · Australian

h encephalitis (MVEV, KUNV) · St. Louis encephalitis (SLEV) ·
r
Flaviviridae West Nile fever (WNV)
o
p Viral hemorrhagic fever: Dengue fever (DV)
o other: Yellow fever (YFV) · Zika fever
d
/
Arbovirus encephalitis: Eastern equine encephalomyelitis
(EEEV) · Western equine encephalomyelitis (WEEV) ·
(
Togaviridae Venezuelan equine encephalomyelitis (VEEV)
a
r other: Chikungunya (CV) · O'Nyong-nyong fever (OV) · Ross
b River fever (RRV)
o
v Viral hemorrhagic fever: Crimean-Congo hemorrhagic fever
Bunyaviridae
i (CCHFV)
r
u
Arbovirus encephalitis: Tick-borne encephalitis (TBEV) ·
s
Tick Powassan encephalitis (PV) · Deer tick virus encephalitis (DTV)
) Flaviviridae
Viral hemorrhagic fever: Omsk hemorrhagic fever (OHFV) ·
Kyasanur forest disease (KFDV/Alkhurma virus)

Reoviridae Colorado tick fever (CTFV)

Viral hemorrhagic fever: Lassa fever (LV) · Venezuelan

hemorrhagic fever (Guanarito virus) · Argentine hemorrhagic
Arenaviridae
fever (Junin virus) · Bolivian hemorrhagic fever (Machupo
Rodent
virus) · Lujo virus
(Robovirus)
M Puumala virus · Andes virus · Sin Nombre virus · Hantavirus
Bunyaviridae
a (HV)
m
m Filoviridae VHF: Ebola hemorrhagic fever · Marburg hemorrhagic fever
a
l Australian bat lyssavirus · Mokola virus · Duvenhage virus ·
Bat Rhabdoviridae
Lagos bat virus · Chandipura virus(sandfly)

Bornaviridae Menangle · Henipavirus · Borna disease (Borna disease virus)

Multiple RhabdoviridaeRabies (RV)

M: VIR virs (prot) cutn/syst (hppv, hiva, drugJ(dnaa, rnaa, rtva,

infl, zost, zoon), epon vacc)

[show]
v•d•e
Infectious skin disease: Viral cutaneous conditions, including viral
exanthema (B00-B09, 050-059)

DNA virus
HSV (Herpes
simplex, Herpetic
whitlow, Herpes
gladiatorum,
Herpetic
keratoconjunctivitis,
Herpetic sycosis,
Neonatal herpes
simplex, Herpes
genitalis, Herpes
labialis, Eczema
herpeticum,
Herpetiform
esophagitis) ·
Alpha
Herpes B virus (B
virus infection)
VZV (Chickenpox,
Herpes zoster,
Herpes zoster oticus,
Herpesviridae Ophthalmic zoster,
Disseminated herpes
zoster, Zoster-
associated pain,
Inflammatory skin
lesions following
zoster infection,
Modified varicella-
like syndrome)

Human herpesvirus
6/Roseolovirus
(Exanthema
Beta subitum, Roseola
vaccinia)
Cytomegalic
inclusion disease

KSHV (Kaposi's
Gamma
sarcoma)

Poxviridae Ortho Variola (Smallpox,

Eczema vaccinatum,
Alastrim) · MoxV
(Monkeypox) · CV
(Cowpox) · VV
 (Vaccinia, Generalized
vaccinia, Progressive
vaccinia)
Buffalopox

Farmyard pox:
Milker's nodule ·
Bovine papular
Para
stomatitis ·
Pseudocowpox · Orf
Sealpox

Yatapoxvirus:
Tanapox · Yaba
Other monkey tumor virus
MCV (Molluscum
contagiosum)

HPV (Wart/Plantar wart,

Heck's disease, Genital wart
(giant), Laryngeal
papillomatosis, Butcher's
wart, Bowenoid papulosis,
Papillomaviridae Epidermodysplasia
verruciformis, Verruca
plana, Pigmented wart,
Verrucae palmares et
plantares )
BPV (Equine sarcoid)

Parvovirus B19 (Erythema

infectiosum,
Parvoviridae Reticulocytopenia, Papular
purpuric gloves and socks
syndrome)

ParamyxoviridaeMeV (Measles)

Rubella virus (Rubella,

Congenital rubella
Togaviridae syndrome) · Alphavirus
infection · Chikungunya
RNA virus fever

CAV (Hand, foot and mouth

disease, Herpangina) ·
Picornaviridae FMDV (Foot-and-mouth
disease) · Boston exanthem
disease
U
n
g
runknown/multiple: Asymmetric periflexural exanthem of childhood · Post-vaccination
ofollicular eruption · Lipschütz ulcer · Eruptive pseudoangiomatosis · Viral-associated
utrichodysplasia · Gianotti–Crosti syndrome
p
e
d

M: VIR virs (prot) cutn/syst (hppv, hiva, drugJ(dnaa, rnaa, rtva,

infl, zost, zoon), epon vacc)

M: INT, anat/phys/devp noco(i,b,d,q,u,r,p,k,c,v)/cong/tumr(n,e,d), proc, drug

SF, LCT sysi/epon (D2/3/4/5/8)

[show]
v•d•e
Infectious diseases - Prion diseases / Transmissible spongiform
encephalopathy (A81, 046)

P
r
i
o
n

d
i
s
e
ainherited/PRNP: fCJD · Gerstmann–Sträussler–Scheinker syndrome · Fatal familial
sinsomnia
esporadic: sCJD
s
acquired/transmissible: Kuru · vCJD
i
n

h
u
m
a
n
s

PBovine spongiform encephalopathy · Scrapie · Chronic wasting disease · Transmissible

rmink encephalopathy
i
o
n

d
i
s
e
a
s
e
s

i
n

a
n
i
m
a
l
s

[show]
v•d•e
Infectious diseases · Mycoses and Mesomycetozoea (B35-B49, 110-118)

S Tinea barbae/Tinea capitis (Kerion) · Tinea

u corporis (Ringworm, Dermatophytid) · Tinea
p cruris · Tinea manuum · Tinea pedis
e (Athlete's foot) · Tinea
r By unguium/Onychomycosis (White superficial
f location onychomycosis · Distal subungual
i onychomycosis · Proximal subungual
c Dermatophyte onychomycosis)
i (Dermatophytosis) Tinea corporis gladiatorum · Tinea faciei ·
aAscomycota Tinea imbricata · Tinea incognito · Favus
l
Epidermophyton floccosum · Microsporum
a canis · Microsporum audouinii ·
n By
Trichophyton interdigitale/mentagrophytes ·
d organism
Trichophyton tonsurans · Trichophyton
schoenleini · Trichophyton rubrum
c
u Hortaea werneckii (Tinea nigra) · Piedraia hortae
t Other
(Black piedra)
a
n
Malassezia furfur (Tinea versicolor, Pityrosporum folliculitis) ·
eBasidiomycota
Trichosporon spp (White piedra)
o
u
s

(
d
e
r
m
a
t
o
m
y
c
o
s
i
s
)
:

T
i
n
e
a
=
s
k
i
n
;

P
i
e
d
r
a

(
e
x
o
t
h
r
i
x
/

e
n
d
o
t
h
r
i
x
)
=
h
a
i
r

S Coccidioides immitis/Coccidioides
u posadasii (Coccidioidomycosis,
b Disseminated coccidioidomycosis, Primary
c cutaneous coccidioidomycosis. Primary
u pulmonary coccidioidomycosis) ·
t Histoplasma capsulatum (Histoplasmosis,
a Onygenales
Primary cutaneous histoplasmosis, Primary
n pulmonary histoplasmosis, Progressive
e Dimorphic disseminated histoplasmosis) · Histoplasma
o (yeast+mold) duboisii (African histoplasmosis) · Lacazia
u loboi (Lobomycosis) · Paracoccidioides
s brasiliensis (Paracoccidioidomycosis)
,
Blastomyces dermatitidis (Blastomycosis,
s North American blastomycosis, South
y Other American blastomycosis) · Sporothrix
s schenckii (Sporotrichosis) · Penicillium
t marneffei (Penicilliosis)
eAscomycota
m Candida albicans (Candidiasis, Oral, Esophageal,
i Vulvovaginal, Chronic mucocutaneous, Antibiotic
c candidiasis, Candidal intertrigo, Candidal
, onychomycosis, Candidal paronychia, Candidid, Diaper
Yeast-like candidiasis, Congenital cutaneous candidiasis, Perianal
a candidiasis, Systemic candidiasis, Erosio interdigitalis
n blastomycetica) · C. glabrata · C. tropicalis · C.
d lusitaniae · Pneumocystis jirovecii (Pneumocystosis,
Pneumocystis pneumonia)
o
p Aspergillus (Aspergillosis, Aspergilloma, Allergic
p bronchopulmonary aspergillosis, Primary cutaneous
o aspergillosis) · Exophiala jeanselmei (Eumycetoma) ·
r Mold-like Fonsecaea pedrosoi/Fonsecaea compacta/Phialophora
t verrucosa (Chromoblastomycosis) · Geotrichum
u candidum (Geotrichosis) · Pseudallescheria boydii
n (Allescheriasis)
i
s
 Cryptococcus neoformans (Cryptococcosis), Trichosporon spp
Basidiomycota
(Trichosporonosis)

Mucorales Rhizopus oryzae · Mucor indicus · Absidia

(Mucormycosis) corymbifera · Syncephalastrum racemosum
t
Zygomycota
i Basidiobolus ranarum
(Zygomycosis)
c Entomophthorales (Basidiobolomycosis) · Conidiobolus
(Entomophthoramycosis) coronatus/Conidiobolus incongruus
(Conidiobolomycosis)

Microsporidia
Enterocytozoon bieneusi/Encephalitozoon intestinalis
(Microsporidiosis)

M
e
s
o
m
y
c
Rhinosporidium seeberi (Rhinosporidiosis)
e
t
o
z
o
e
a

U
n
g
r
Alternariosis · Fungal folliculitis · Fusarium (Fusariosis) · Granuloma gluteale
o
infantum · Hyalohyphomycosis · Otomycosis · Phaeohyphomycosis
u
p
e
d

M: MYC fung, clas fung drug (fung)

[show]
v•d•e
Infectious diseases - Parasitic disease: protozoan infection: Amoebozoa
diseases (A06, 006)

L
Centramoebida Acanthamoeba (Acanthamoeba keratitis, Cutaneous acanthamoebiasis,
o Granulomatous amoebic encephalitis, Acanthamoeba infection)
b
o Balamuthia mandrillaris (Balamuthia amoebic encephalitis, Balamuthia
s infection)
e
aFlabellinea Sappinia diploidea/Sappinia pedata (Sappinia amoebic encephalitis)

(
f
r
e
e
-
l
i
v
i
n
g
)

C
o
n
o
s
a
/
A
Entamoeba histolytica (Entamoebiasis, Amoebic dysentery, Amoebic liver abscess,
r
Cutaneous entamoebiasis, Amoebic brain abscess, Amebiasis cutis) · Entamoeba
c
gingivalis
h
a
m
o
e
b
a
e

M: PRO ambz, excv, chrm ambz, excv, chrm ambz, excv, chrm
(strc)

[show]
v•d•e
Infectious diseases – Parasitic disease: protozoan infection: Excavata (A06-
A07, B55-B57, 007, 085-086)

D
Trypanosomatida T. brucei (African trypanosomiasis) · T. cruzi (Chagas
i Trypanosomiasis
disease)
s
c Leishmaniasis Leishmania major/L. mexicana/L. aethiopica/L.
i tropica (Cutaneous leishmaniasis) · L. braziliensis
c
r (Mucocutaneous leishmaniasis) · L.
i donovani/infantum (Visceral leishmaniasis)
s
tSchizopyrenida Naegleria fowleri (Primary amoebic meningoencephalitis)
a
t
a

TDiplomonadida Giardia lamblia (Giardiasis)

r
i Trichomonas vaginalis (Trichomoniasis) · Dientamoeba fragilis
cTrichomonadida (Dientamoebiasis)
h
o
z
o
a

M: PRO ambz, excv, chrm ambz, excv, chrm ambz, excv, chrm
(strc)

[show]
v•d•e
Infectious diseases - Parasitic disease: protozoan infection: Chromalveolate
and Archaeplastida (A07, B50-B54,B58, 007, 084)

Coccidia: Cryptosporidium
C
hominis/Cryptosporidium parvum
h
Conoidasida/ (Cryptosporidiosis) · Isospora belli
r
Coccidia (Isosporiasis) · Cyclospora cayetanensis
o
(Cyclosporiasis) · Toxoplasma gondii
m Apicomplexa (Toxoplasmosis)
a
Alveolate
l
v Plasmodium falciparum/vivax/ovale/malariae
e Aconoidasida (Malaria, Blackwater fever)
o Babesia (Babesiosis)
l
a
Ciliophora Balantidium coli (Balantidiasis)
t
e
HeterokontBlastocystis (Blastocystosis)

A
Algaemia: Prototheca wickerhamii (Protothecosis)
r
c
h
a
e
p
l
a
s
t
i
d
a

M: PRO ambz, excv, chrm ambz, excv, chrm ambz, excv, chrm
(strc)

[show]
v•d•e
Infectious diseases · Parasitic disease: helminthiases (B65–B83, 120–129)

F Blood Schistosoma mansoni/japonicum/mekongi/haematobium

l fluke (Schistosomiasis) · Trichobilharzia regenti (Swimmer's itch)
a
t Liver Clonorchis sinensis (Clonorchiasis) · Fasciola
wFluke/trematodefluke hepatica/gigantica (Fascioliasis) · Opisthorchis
o(Trematode
rinfection) Lung
m Paragonimus westermani (Paragonimiasis)
fluke
/
Intestinal
p Fasciolopsis buski (Fasciolopsiasis)
fluke
l
a
Echinococcus granulosus/Echinococcus multilocularis
t
(Echinococcosis) · Taenia saginata (beef)/Taenia
y
Cyclophyllidea asiatica/Taenia solium (pork)
h
Cestoda (Taeniasis/Cysticercosis) · Hymenolepis
e
(Tapeworm nana/Hymenolepis diminuta (Hymenolepiasis)
l
infection)
m
Diphyllobothrium latum (Diphyllobothriasis) ·
i
Pseudophyllidea Spirometra erinaceieuropaei (Sparganosis) ·
n
Diphyllobothrium mansonoides (Sparganosis)
t
h

R
Secernentea Spirurida CamallaninaDracunculus medinensis (Dracunculiasis)
o
u Spirurina
n Onchocerca volvulus
d (Onchocerciasis) · Loa loa (Loa loa
w filariasis) · Mansonella
Filarioidea
o (Mansonelliasis) · Dirofilaria repens
(Filariasis)
r (Dirofilariasis)
m Wuchereria bancrofti · Brugia
/ malayi · Brugia timori

n Thelazioidea Gnathostoma
e
m spinigerum/Gnathostoma hispidum
a (Gnathostomiasis) · Thelazia
t (Thelaziasis)
o
d Spiruroidea Gongylonema
e
Ancylostoma duodenale/Ancylostoma braziliense
(
Strongylida (Ancylostomiasis, Cutaneous larva migrans) · Necator
N
(hookworm) americanus (Necatoriasis) · Angiostrongylus cantonensis
e
(Angiostrongyliasis) · Metastrongylus (Metastrongylosis)
m
a
Ascaris lumbricoides (Ascariasis) · Anisakis (Anisakiasis) ·
t
Ascaridida Toxocara canis/Toxocara cati (Visceral larva
o
migrans/Toxocariasis) · Baylisascaris
d
e
Rhabditida Strongyloides stercoralis (Strongyloidiasis)
i
n Oxyurida Enterobius vermicularis (Enterobiasis · Pinworm)
f
e Trichinella spiralis (Trichinosis) · Trichuris trichiura (Trichuriasis ·
Adenophorea
c Whipworm) · Capillaria philippinensis (Intestinal capillariasis) ·
t Capillaria hepatica
i
o
n
)

M: IFT helm,arth (acar) helm, arth (lice), zoon helm, arth

[show]
v•d•e
Infectious diseases - Parasitic disease: ectoparasitic infestation / arthropod
(B85-B89, 132-134)

Pediculus humanus corporis/Pediculus humanus capitis (Pediculosis,

IPhthiraptera Head-louse infestation, Pediculosis corporis)
n Phthirus pubis (Phthiriasis)
s
eHemiptera Cimex (Cimicosis)
c
tDiptera Dermatobia hominis/Cordylobia anthropophaga (Myiasis)
a
SiphonapteraTunga penetrans (Tungiasis)

AAcariasis/mangeTrombidiformes: Trombicula (Trombiculosis, Chigger bite) · Demodex

r(mites) brevis/Demodex folliculorum (Demodicosis, Demodex mite bite) ·
a Pyemotes herfsi · Cheyletiella (Cheyletiellosis)
c
h Sarcoptiformes: Sarcoptes scabiei (Scabies)
n
i Parasitiformes: Dermanyssus gallinae · Liponyssoides sanguineus
d
aTicks Tick infestation

C Linguatula serrata (Linguatulosis) · Porocephalus crotali/Armillifer

rPentastomida armillatus (Porocephaliasis)
u
s
t
a
c
e
a

M: IFT helm,arth (acar) helm, arth (lice), zoon helm, arth

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10_Chapter_I:_Certain_infectious_and_parasitic_diseases"
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ICD-10 Chapter II: Neoplasms

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International Statistical Classification of Diseases and Related Health Problems 10th
Revision
Chapter Blocks Title
I A00-B99 Certain infectious and parasitic diseases
C00-
II Neoplasms
D48
D50- Diseases of the blood and blood-forming organs and certain disorders
III
D89 involving the immune mechanism
IV E00-E90 Endocrine, nutritional and metabolic diseases
V F00-F99 Mental and behavioural disorders
G00-
VI Diseases of the nervous system
G99
H00-
VII Diseases of the eye and adnexa
H59
H60-
VIII Diseases of the ear and mastoid process
H95
IX I00-I99 Diseases of the circulatory system
X J00-J99 Diseases of the respiratory system
K00-
XI Diseases of the digestive system
K93
XII L00-L99 Diseases of the skin and subcutaneous tissue
M00-
XIII Diseases of the musculoskeletal system and connective tissue
M99
N00-
XIV Diseases of the genitourinary system
N99
O00-
XV Pregnancy, childbirth and the puerperium
O99
XVI P00-P96 Certain conditions originating in the perinatal period
Q00- Congenital malformations, deformations and chromosomal
XVII
Q99 abnormalities
Symptoms, signs and abnormal clinical and laboratory findings, not
XVIII R00-R99
elsewhere classified
XIX S00-T98 Injury, poisoning and certain other consequences of external causes
V01-
XX External causes of morbidity and mortality
Y98
XXI Z00-Z99 Factors influencing health status and contact with health services
U00-
XXII Codes for special purposes
U99
The International Statistical Classification of Diseases and Related Health Problems 10th
Revision (ICD-10) is a coding of diseases and signs, symptoms, abnormal findings,
complaints, social circumstances and external causes of injury or diseases, as classified
by the World Health Organization (WHO).[1]. This page contains ICD-10 Chapter II:
Neoplasms.

Contents
[hide]
• 1 C00-D48 - Neoplasms
 ○ 1.1 (C00-C14) Malignant neoplasms, lip, oral cavity and pharynx
○ 1.2 (C15-C26) Malignant neoplasms, digestive organs
○ 1.3 (C30-C39) Malignant neoplasms, respiratory system and intrathoracic
organs
○ 1.4 (C40-C41) Malignant neoplasms, bone and articular cartilage
○ 1.5 (C43-C44) Malignant neoplasms, skin
○ 1.6 (C45-C49) Malignant neoplasms, connective and soft tissue
○ 1.7 (C50-C58) Malignant neoplasms, breast and female genital organs
○ 1.8 (C60-C63) Malignant neoplasms, male genital organs
○ 1.9 (C64-C68) Malignant neoplasms, urinary organs
○ 1.10 (C69-C72) Malignant neoplasms, eye, brain and central nervous
system
○ 1.11 (C73-C75) Malignant neoplasms, endocrine glands and related
structures
○ 1.12 (C76-C80) Malignant neoplasms, secondary and ill-defined
○ 1.13 (C81-C96) Malignant neoplasms, stated or presumed to be primary,
of lymphoid, haematopoietic and related tissue
○ 1.14 (C97) Malignant neoplasms of independent (primary) multiple sites
○ 1.15 (D00-D09) In situ neoplasms
○ 1.16 (D10-D36) Benign neoplasms
○ 1.17 (D37-D48) Neoplasms of uncertain or unknown behaviour
• 2 See also
• 3 References

[edit] C00-D48 - Neoplasms

[edit] (C00-C14) Malignant neoplasms, lip, oral cavity and pharynx
• (C00.) Malignant neoplasm of lip
• (C01.) Malignant neoplasm of base of tongue
• (C02.) Malignant neoplasm of other and unspecified parts of tongue
• (C03.) Malignant neoplasm of gum
• (C04.) Malignant neoplasm of floor of mouth
• (C05.) Malignant neoplasm of palate
• (C06.) Malignant neoplasm of other and unspecified parts of mouth
• (C07.) Malignant neoplasm of parotid gland
• (C08.) Malignant neoplasm of other and unspecified major salivary glands
• (C09.) Malignant neoplasm of tonsil
• (C10.) Malignant neoplasm of oropharynx
• (C11.) Malignant neoplasm of nasopharynx
 • (C12.) Malignant neoplasm of piriform sinus
• (C13.) Malignant neoplasm of hypopharynx
• (C14.) Malignant neoplasm of other and ill-defined sites in the lip, oral cavity and
pharynx
[edit] (C15-C26) Malignant neoplasms, digestive organs
• (C15.) Malignant neoplasm of Esophagus
• (C16.) Malignant neoplasm of Stomach
○ (C16.0) Cardia
○ (C16.1) Fundus of stomach
○ (C16.2) Body of stomach
○ (C16.3) Pyloric antrum
○ (C16.4) Pylorus
○ (C16.5) Lesser curvature of stomach, unspecified
○ (C16.6) Greater curvature of stomach, unspecified
○ (C16.8) Overlapping lesion of stomach
○ (C16.9) Stomach, unspecified
• (C17.) Malignant neoplasms of small intestine
○ (C17.0) Duodenum
○ (C17.1) Jejunum
○ (C17.2) Ileum
○ (C17.3) Meckel's diverticulum
○ (C17.8) Overlapping lesion of small intestine
○ (C17.9) Small intestine, unspecified
• (C18.) Malignant neoplasm of colon
○ (C18.0) Caecum
○ (C18.1) Appendix
○ (C18.2) Ascending colon
○ (C18.3) Hepatic flexure
○ (C18.4) Transverse colon
○ (C18.5) Splenic flexure
○ (C18.6) Descending colon
○ (C18.7) Sigmoid colon
○ (C18.8) Overlapping lesion of colon
○ (C18.9) Colon, unspecified
• (C19.) Malignant neoplasm of rectosigmoid junction
• (C20.) Malignant neoplasm of rectum
• (C21.) Malignant neoplasms of anus and anal canal
 • (C22.) Malignant neoplasms of liver and intrahepatic bile ducts
○ (C22.0) Liver cell carcinoma
○ (C22.1) Intrahepatic bile duct carcinoma
○ (C22.2) Hepatoblastoma
○ (C22.3) Angiosarcoma of liver
○ (C22.4) Other sarcomas of liver
○ (C22.7) Other specified carcinomas of liver
○ (C22.9) Liver, unspecified
• (C23.) Malignant neoplasm of gallbladder
• (C24.) Malignant neoplasm of other and unspecified parts of biliary tract
• (C25.) Malignant neoplasm of pancreas
○ (C25.0) Head of pancreas
○ (C25.1) Body of pancreas
○ (C25.2) Tail of pancreas
○ (C25.3) Pancreatic duct
○ (C25.4) Endocrine pancreas
○ (C25.7) Other parts of pancreas
○ (C25.8) Overlapping lesion of pancreas
○ (C25.9) Pancreas, unspecified
• (C26.) Malignant neoplasms of other and ill-defined Digestive Organs
[edit] (C30-C39) Malignant neoplasms, respiratory system and
intrathoracic organs
• (C30.) Malignant neoplasm of nasal cavity and middle ear
○ (C30.0) Nasal cavity
○ (C30.1) Middle ear
• (C31.) Malignant neoplasm of accessory sinuses
• (C32.) Malignant neoplasm of larynx
• (C33.) Malignant neoplasm of trachea
• (C34.) Malignant neoplasm of bronchus and lung
○ (C34.0) Main bronchus
○ (C34.1) Upper lobe, bronchus or lung
 Pancoast tumor
○ (C34.2) Middle lobe, bronchus or lung
○ (C34.3) Lower lobe, bronchus or lung
○ (C34.8) Overlapping lesion of bronchus and lung
• (C37.) Malignant neoplasm of thymus
• (C38.) Malignant neoplasm of heart, mediastinum and pleura
 ○ (C38.0) Heart
○ (C38.1) Anterior mediastinum
○ (C38.2) Posterior mediastinum
○ (C38.3) Mediastinum, part unspecified
○ (C38.4) Pleura
○ (C38.8) Overlapping lesion of heart, mediastinum and pleura
• (C39.) Malignant neoplasms of other and ill-defined sites in respiratory system
and intrathoracic organs
[edit] (C40-C41) Malignant neoplasms, bone and articular cartilage
• (C40.) Malignant neoplasm of bone and articular cartilage of limbs
• (C41.) Malignant neoplasm of bone and articular cartilage of other and
unspecified sites
(Note: ICD-10 and ICD-O topography codes are usually the same, but C42 is used in
ICD-O but not ICD-10.)[2]
[edit] (C43-C44) Malignant neoplasms, skin
• (C43.) Malignant melanoma of Skin
• (C44.) Other malignant neoplasms of skin
[edit] (C45-C49) Malignant neoplasms, connective and soft tissue
• (C45.) Mesothelioma
• (C46.) Kaposi's Sarcoma
• (C47.) Malignant neoplasm of peripheral nerves and autonomic nervous system
• (C48.) Malignant neoplasm of retroperitoneum and peritoneum
○ (C48.0) Retroperitoneum
○ (C48.1) Specified parts of peritoneum
○ (C48.2) Peritoneum, unspecified
• (C49.) Malignant neoplasm of other connective and soft tissue
○ C49.M10 Malignant fibrous histiocytoma
○ C49.M12 Atypical fibroxanthoma
○ C49.M20 Haemangiopericytoma
○ C49.M22 Angioendotheliomatosis, malignant
○ C49.M24 Dermatofibrosarcoma protruberans
○ C49.M30 Bednar tumour
○ C49.M40 Sarcoma of skin
○ C49.M42 Fibrosarcoma
○ C49.M44 Schwannoma, malignant
○ C49.M48 Leiomyosarcoma
○ C49.M50 Rhabdomyosarcoma
○ C49.M54 Myxofibrosarcoma
 ○ C49.M60 Angiosarcoma, cutaneous
○ C49.M70 Lymphangiosarcoma
(Alphanumeric subcodes are ILDS.)
[edit] (C50-C58) Malignant neoplasms, breast and female genital organs
• (C50.) Malignant neoplasm of breast
• (C51.) Malignant neoplasm of vulva
• (C52.) Malignant neoplasm of vagina
• (C53.) Malignant neoplasm of cervix uteri
• (C54.) Malignant neoplasm of corpus uteri
○ (C54.1) Endometrial cancer
• (C55.) Malignant neoplasm of uterus, part unspecified
• (C56.) Malignant neoplasm of ovary
• (C57.) Malignant neoplasms of other and unspecified female and genital organs
• (C58.) Malignant neoplasm of placenta
○ Choriocarcinoma NOS
○ Chorionepithelioma NOS
[edit] (C60-C63) Malignant neoplasms, male genital organs
• (C60.) Malignant neoplasm of penis
• (C61.) Malignant neoplasm of prostate
• (C62.) Malignant neoplasm of testis
• (C63.) Malignant neoplasm of other and unspecified male genital organs
[edit] (C64-C68) Malignant neoplasms, urinary organs
• (C64.) Malignant neoplasm of kidney, except renal pelvis
○ Wilms' tumor
• (C65.) Malignant neoplasm of renal pelvis
• (C66.) Malignant neoplasm of ureter
• (C67.) Malignant neoplasm of bladder
• (C68.) Malignant neoplasm of other and unspecified urinary organs
[edit] (C69-C72) Malignant neoplasms, eye, brain and central nervous
system
• (C69.) Malignant neoplasms of eye and adnexa
○ (C69.0) Conjunctiva
○ (C69.1) Cornea
○ (C69.2) Retina
 Retinoblastoma
○ (C69.3) Choroid
○ (C69.4) Ciliary body
 ○ (C69.5) Lacrimal gland and duct
○ (C69.6) Orbit
○ (C69.7) Overlapping lesion of eye and adnexa
• (C70.) Malignant neoplasm of meninges
○ (C70.0) Cerebral meninges
○ (C70.1) Spinal meninges
• (C71.) Malignant neoplasm of brain
○ (C71.0) Cerebrum, except lobes and ventricles
○ (C71.1) Frontal lobe
○ (C71.2) Temporal lobe
○ (C71.3) Parietal lobe
○ (C71.4) Occipital lobe
○ (C71.5) Cerebral ventricle
○ (C71.6) Cerebellum
○ (C71.7) Brain stem
○ (C71.8) Overlapping lesion of brain
○ (C71.9) Brain, unspecified
• (C72.) Malignant neoplasm of spinal cord, cranial nerves and other parts of
central nervous system
○ (C72.0) Spinal cord
○ (C72.1) Cauda equina
○ (C72.2) Olfactory nerve
○ (C72.3) Optic nerve
○ (C72.4) Acoustic nerve
○ (C72.5) Other and unspecified cranial nerves
○ (C72.8) Overlapping lesion of brain and other parts of central nervous
system
○ (C72.9) Central nervous system, unspecified
[edit] (C73-C75) Malignant neoplasms, endocrine glands and related
structures
• (C73.) Malignant neoplasm of thyroid gland
• (C74.) Malignant neoplasm of adrenal gland
○ (C74.0) Cortex of adrenal gland
○ (C74.1) Medulla of adrenal gland
 Pheochromocytoma
○ (C74.9) Adrenal gland, unspecified
 Neuroblastoma, NOS
• (C75.) Malignant neoplasm of other endocrine glands and related structures
[edit] (C76-C80) Malignant neoplasms, secondary and ill-defined
• (C76.) Malignant neoplasm of other and ill-defined sites
○ (C76.0) Langerhans' cell histiocytosis, not elsewhere classified
○ (C76.1) Haemophagocytic lymphohistiocytosis
○ (C76.2) Haemophagocytic syndrome, infection-associated
○ (C76.3) Other histiocytosis syndromes
• (C77.) Secondary and unspecified malignant neoplasm of lymph nodes
• (C78.) Secondary malignant neoplasm of respiratory and digestive organs
• (C79.) Secondary malignant neoplasm of other sites
• (C80.) Malignant neoplasm without specification of site
[edit] (C81-C96) Malignant neoplasms, stated or presumed to be primary,
of lymphoid, haematopoietic and related tissue
• (C81.) Hodgkin's Disease
○ (C81.0) Lymphocytic predominance
○ (C81.1) Nodular sclerosis
○ (C81.2) Mixed cellularity
○ (C81.3) Lymphocytic depletion
• (C82.) Follicular non-Hodgkin's lymphoma (nodular)
○ (C82.0) Small cleaved cell, follicular
○ (C82.1) Mixed small cleaved and large cell, follicular
○ (C82.2) Large cell, follicular
• (C83.) Diffuse non-Hodgkin's lymphoma
○ (C83.0) Small cell (diffuse)
○ (C83.1) Small cleaved cell (diffuse)
○ (C83.2) Mixed small and large cell (diffuse)
○ (C83.3) Large cell (diffuse)
○ (C83.4) Immunoblastic (diffuse)
○ (C83.5) Lymphoblastic (diffuse)
○ (C83.6) Undifferentiated (diffuse)
○ (C83.7) Burkitt's tumour
• (C84.) Peripheral and cutaneous T-cell lymphomas
○ (C84.0) Mycosis fungoides
○ (C84.1) Sézary's disease
○ (C84.2) T-zone lymphoma
○ (C84.3) Lymphoepithelioid lymphoma
○ (C84.4) Peripheral T-cell lymphoma
• (C85.) Other and unspecified types of non-Hodgkin's lymphoma
 ○ (C85.0) Lymphosarcoma
○ (C85.1) B-cell lymphoma, unspecified
• (C88.) Malignant immunoproliferative diseases
○ (C88.0) Waldenström's macroglobulinaemia
○ (C88.1) Alpha heavy chain disease
○ (C88.2) Gamma heavy chain disease
○ (C88.3) Immunoproliferative small intestinal disease
• (C90.) Multiple myeloma and malignant plasma cell neoplasms
○ (C90.0) Multiple myeloma
○ (C90.1) Plasma cell leukaemia
○ (C90.2) Plasmacytoma, extramedullary
• (C91.) Lymphoid leukaemia
○ (C91.0) Acute lymphoblastic leukaemia
○ (C91.1) Chronic lymphocytic leukaemia
○ (C91.4) Hairy-cell leukaemia
• (C92.) Myeloid leukaemia
○ (C92.0) Acute myeloid leukaemia
○ (C92.1) Chronic myeloid leukaemia
○ (C92.2) Subacute myeloid leukaemia
○ (C92.3) Myeloid sarcoma
 Chloroma
 Granulocytic sarcoma
○ (C92.4) Acute promyelocytic leukaemia
○ (C92.5) Acute myelomonocytic leukaemia
• (C93.) Monocytic leukaemia
○ (C93.0) Acute monocytic leukaemia
○ (C93.1) Chronic monocytic leukaemia
○ (C93.2) Subacute monocytic leukaemia
• (C94.) Other leukaemias of specified cell type
○ (C94.0) Acute erythraemia and erythroleukaemia
 Di Guglielmo's disease
○ (C94.1) Chronic erythraemia
○ (C94.2) Acute megakaryoblastic leukaemia
○ (C94.3) Mast cell leukaemia
○ (C94.4) Acute panmyelosis
○ (C94.5) Acute myelofibrosis
○ (C94.7) Other specified leukaemias
 • (C95.) Leukaemia of unspecified cell type
○ (C95.0) Acute leukaemia of unspecified cell type
○ (C95.1) Chronic leukaemia of unspecified cell type
○ (C95.2) Subacute leukaemia of unspecified cell type
○ (C95.7) Other leukaemia of unspecified cell type
○ (C95.9) Leukaemia, unspecified
• (C96.) Other and unspecified malignant neoplasms of lymphoid, haematopoietic
and related tissue
○ (C96.0) Letterer-Siwe disease
○ (C96.1) Malignant histiocytosis
○ (C96.2) Malignant mast cell tumour
 Malignant mastocytosis
○ (C96.3) True histiocytic lymphoma
○ (C96.7) Other specified malignant neoplasms of lymphoid,
haematopoietic and related tissue
○ (C96.9) Malignant neoplasm of lymphoid, haematopoietic and related
tissue, unspecified
[edit] (C97) Malignant neoplasms of independent (primary) multiple sites
• (C97.) Malignant neoplasms of independent (primary) multiple sites
[edit] (D00-D09) In situ neoplasms
• (D00.) Carcinoma in situ of oral cavity, oesophagus and stomach
• (D01.) Carcinoma in situ of other and unspecified digestive organs
• (D02.) Carcinoma in situ of middle ear and respiratory system
• (D03.) Melanoma in situ
• (D04.) Carcinoma in situ of skin
• (D05.) Carcinoma in situ of breast
• (D06.) Carcinoma in situ of cervix uteri
• (D07.) Carcinoma in situ of other and unspecified genital organs
• (D09.) Carcinoma in situ of other and unspecified sites
[edit] (D10-D36) Benign neoplasms
• (D10.) Benign neoplasm of mouth and pharynx
• (D11.) Benign neoplasm of major salivary glands
○ Warthin's tumor
○ Pleomorphic adenoma
○ (D11.0) Parotid gland
○ (D11.7) Other major salivary glands
 Sublingual gland
 Submandibular gland
 ○ (D11.9) Major salivary gland, unspecified
• (D12.) Benign neoplasm of colon, rectum, anus and anal canal
○ Familial adenomatous polyposis
○ (D12.0) Caecum
○ (D12.1) Appendix
○ (D12.2) Ascending colon
○ (D12.3) Transverse colon
○ (D12.4) Descending colon
○ (D12.5) Sigmoid colon
○ (D12.6) Colon, unspecified
 Adenomatosis of colon
○ (D12.7) Rectosigmoid junction
○ (D12.8) Rectum
○ (D12.9) Anus and anal canal
• (D13.) Benign neoplasm of other and ill-defined parts of digestive system
○ (D13.0) Oesophagus
○ (D13.1) Stomach
○ (D13.2) Duodenum
○ (D13.3) Other and unspecified parts of small intestine
○ (D13.4) Liver
 Intrahepatic bile ducts
○ (D13.5) Extrahepatic bile ducts
○ (D13.6) Pancreas
○ (D13.7) Endocrine pancreas
 Islet cell tumour
 Islets of Langerhans
○ (D13.9) Ill-defined sites within the digestive system
 Digestive system NOS
 Intestine NOS
 Spleen
• (D14.) Benign neoplasm of middle ear and respiratory system
○ (D14.0) Middle ear, nasal cavity and accessory sinuses
○ (D14.1) Larynx
○ (D14.2) Trachea
○ (D14.3) Bronchus and lung
○ (D14.4) Respiratory system, unspecified
• (D15.) Benign neoplasm of other and unspecified intrathoracic organs
 ○ (D15.0) Thymus
○ (D15.1) Heart
 Myxoma
○ (D15.2) Mediastinum
• (D16.) Benign neoplasm of bone and articular cartilage
○ (D16.0) Scapula and long bones of upper limb
○ (D16.1) Short bones of upper limb
○ (D16.2) Long bones of lower limb
○ (D16.3) Short bones of lower limb
○ (D16.4) Bones of skull and face
○ (D16.5) Lower jaw bone
○ (D16.6) Vertebral column
○ (D16.7) Ribs, sternum and clavicle
○ (D16.8) Pelvic bones, sacrum and coccyx
○ (D16.9) Bone and articular cartilage, unspecified
• (D17.) Benign lipomatous neoplasm
○ Lipoma (ILDS D17.910)
○ Lipomata, multiple (ILDS D17.920)
○ Angiolipoma (ILDS D17.930)
○ Lipoblastomatosis (ILDS D17.940)
○ Hibernoma (ILDS D17.950)
• (D18.) Haemangioma and lymphangioma, any site
○ (D18.0) Haemangioma, any site
 Angioma NOS
○ (D18.1) Lymphangioma, any site
 Cavernous haemangioma (ILDS D18.014)
• (D19.) Benign neoplasm of mesothelial tissue
• (D20.) Benign neoplasm of soft tissue of retroperitoneum and peritoneum
• (D21.) Other benign neoplasms of connective and other soft tissue
○ Chondroma
○ Masson's pseudoangiosarcoma (ILDS D21.M20)
○ Synovioma, giant-cell (ILDS D21.M30)
○ Leiomyoma (ILDS D21.M40)
○ Rhabdomyoma (ILDS D21.M50)
○ Angioleiomyoma (ILDS D21.M60)
• (D22.) Melanocytic naevi
• (D23.) Other benign neoplasms of skin
 • (D24.) Benign neoplasm of breast
• (D25.) Leiomyoma of uterus
○ Uterine fibroids
• (D26.) Other benign neoplasms of uterus
• (D27.) Benign neoplasm of ovary
• (D28.) Benign neoplasm of other and unspecified female genital organs
• (D29.) Benign neoplasm of male genital organs
• (D30.) Benign neoplasm of urinary organs
○ (D30.0) Kidney
○ (D30.1) Renal pelvis
○ (D30.2) Ureter
○ (D30.3) Urinary bladder
○ (D30.4) Urethra
○ (D30.7) Other urinary organs
○ (D30.9) Urinary organ, unspecified
• (D31.) Benign neoplasm of eye and adnexa
• (D32.) Benign neoplasm of meninges
• (D33.) Benign neoplasm of brain and other parts of central nervous system
• (D34.) Benign neoplasm of thyroid gland
• (D35.) Benign neoplasm of other and unspecified endocrine glands
○ (D35.0) Adrenal gland
○ (D35.1) Parathyroid gland
○ (D35.2) Pituitary gland
 Pituitary adenoma
 Prolactinoma
○ (D35.3) Craniopharyngeal duct
○ (D35.4) Pineal gland
○ (D35.5) Carotid body
○ (D35.6) Aortic body and other paraganglia
○ (D35.7) Other specified endocrine glands
○ (D35.8) Pluriglandular involvement
○ (D35.9) Endocrine gland, unspecified
• (D36.) Benign neoplasm of other and unspecified sites
[edit] (D37-D48) Neoplasms of uncertain or unknown behaviour
• (D37.) Neoplasm of uncertain or unknown behaviour of oral cavity and digestive
organs
• (D38.) Neoplasm of uncertain or unknown behaviour of middle ear and
respiratory and intrathoracic organs
• (D39.) Neoplasm of uncertain or unknown behaviour of female genital organs
○ (D39.0) Uterus
○ (D39.1) Ovary
○ (D39.2) Placenta
○ (D39.7) Other female genital organs
○ (D39.9) Female genital organ, unspecified
• (D40.) Neoplasm of uncertain or unknown behaviour of male genital organs
• (D41.) Neoplasm of uncertain or unknown behaviour of urinary organs
• (D42.) Neoplasm of uncertain or unknown behaviour of meninges
• (D43.) Neoplasm of uncertain or unknown behaviour of brain and central nervous
system
• (D44.) Neoplasm of uncertain or unknown behaviour of endocrine glands
○ (D44.0) Thyroid gland
○ (D44.1) Adrenal gland
○ (D44.2) Parathyroid gland
○ (D44.3) Pituitary gland
○ (D44.4) Craniopharyngeal duct
○ (D44.5) Pineal gland
○ (D44.6) Carotid body
○ (D44.7) Aortic body and other paraganglia
○ (D44.8) Pluriglandular involvement
 Multiple endocrine adenomatosis
○ (D44.9) Endocrine gland, unspecified
• (D45.) Polycythaemia vera
• (D46.) Myelodysplastic syndromes
• (D47.) Other neoplasms of uncertain or unknown behaviour of lymphoid,
haematopoietic and related tissue
○ (D47.0) Histiocytic and mast cell tumours of uncertain and unknown
behaviour
 Mast cell tumour NOS
 Mastocytoma NOS
○ (D47.1) Chronic myeloproliferative disease
 Myelofibrosis (with myeloid metaplasia)
 Myeloproliferative disease, unspecified
 Myelosclerosis (megakaryocytic) with myeloid metaplasia
○ (D47.2) Monoclonal gammopathy
○ (D47.3) Essential (haemorrhagic) thrombocythaemia
 ○ (D47.7) Other specified neoplasms of uncertain or unknown behaviour of
lymphoid, haematopoietic and related tissue
○ (D47.9) Neoplasm of uncertain or unknown behaviour of lymphoid,
haematopoietic and related tissue, unspecified
• (D48.) Neoplasm of uncertain or unknown behaviour of other and unspecified
sites
○ (D48.0) Bone and articular cartilage
○ (D48.1) Connective and other soft tissue
○ (D48.2) Peripheral nerves and autonomic nervous system
○ (D48.3) Retroperitoneum
○ (D48.4) Peritoneum
○ (D48.5) Skin
○ (D48.6) Breast
○ (D48.7) Other specified sites
○ (D48.9) Neoplasm of uncertain or unknown behaviour, unspecified

[edit] See also

• List of ICD-10 codes
• International Statistical Classification of Diseases and Related Health Problems
[edit] References
1. ^ WHO | International Classification of Diseases (ICD)
2. ^ http://training.seer.cancer.gov/coding/differences/other.html
[show]
v•d•e
Pathology: Medical conditions and ICD code

(Disease / Disorder / Illness, Syndrome / Sequence, Symptom / Sign, Injury, etc.)

(
A
/
B
,

0Infectious disease/Infection: Bacterial disease (G+, G-) · Virus disease · Parasitic disease
0(Protozoan infection, Helminthiasis, Ectoparasitic infestation) · Mycosis · Zoonosis
1
-
1
3
9
)

(Cancer Tumor
C(C00-D48,
/140-239)
D
,Myeloid
hematologic
1(D50-D77, Anemia · Coagulopathy
4280-289)
0
-Lymphoid
2immune
3(D80-D89, Immunodeficiency · Immunoproliferative disorder · Hypersensitivity
9279)

&

2
7
9
-
2
8
9
)

(
E
,

2
4
Endocrine disease · Nutrition disorder · Inborn error of metabolism
0
-
2
7
8
)

(
F
,

2
9
Mental disorder
0
-
3
1
9
)

(Nervous system disease (CNS, PNS) · Neuromuscular disease

G
,

3
2
0
-
3
5
9
)

(
H
,

3
6
Eye disease · Ear disease
0
-
3
8
9
)

(
I
,

3
9
Cardiovascular disease (Heart disease, Vascular disease)
0
-
4
5
9
)

(
J
,

4
6
Respiratory disease (Obstructive lung disease, Restrictive lung disease, Pneumonia)
0
-
5
1
9
)
(
K
,

5
2Stomatognathic disease (Tooth disease) · Digestive disease (Esophageal, Stomach,
0Enteropathy, Liver, Pancreatic)
-
5
7
9
)

(
L
,

6
8
Skin disease · skin appendages (Nail disease, Hair disease, Sweat gland disease)
0
-
7
0
9
)

(
M
,

7
1Musculoskeletal disorders: Myopathy · Arthropathy · Osteochondropathy (Osteopathy,
0Chondropathy)
-
7
3
9
)

(
N
,

5
8Urologic disease (Nephropathy, Urinary bladder disease) · Male genital disease · Breast
0disease · Female genital disease
-
6
2
9
)
(
O
,

6
3
Complications of pregnancy · Obstetric labor complication · Puerperal disorder
0
-
6
7
9
)

(
P
,

7
6
Fetal disease
0
-
7
7
9
)

(
Q
,

7
4
Congenital disorder (Congenital abnormality)
0
-
7
5
9
)

(Syndromes · Medical signs (Eponymous)

R
,

7
8
0
-
7
9
9
)

(
S
/
T
,

8Bone fracture · Joint dislocation · Sprain · Strain · Subluxation · Head injury · Chest
0trauma · Poisoning
0
-
9
9
9
)

[show]
v•d•e
Tumors of lip, oral cavity and pharynx / head and neck cancer (C00-
C14/D10-D11, 140-149/210)

O malignant epithelial tumors (Acinic cell carcinoma, Mucoepidermoid

r carcinoma, Adenoid cystic carcinoma)
aSalivary
lgland benign epithelial tumors (Pleomorphic adenoma, Warthin's tumor)
ungrouped: Oncocytoma · Polymorphous low-grade adenocarcinoma
c
aTongue Leukoplakia · Rhabdomyoma
n
c
e
r

M: MOU anat/devp noco/cofa(c)/cogi/tumr, proc (peri), drug

sysi (A1)

[show]
v•d•e
Tumors: digestive system neoplasia (C15-C26/D12-D13, 150-159/211)

G EsophagusSquamous cell carcinoma · Adenocarcinoma

IUpper
GI
Gastric carcinoma · Signet ring cell carcinoma · Gastric lymphoma
ttract Stomach (MALT lymphoma) · Linitis plastica
r
aLowerSmall
cGI Duodenal cancer (Adenocarcinoma)
intestine
ttract
Appendix Carcinoid · Pseudomyxoma peritonei
 colorectal polyp: Peutz-Jeghers syndrome · Juvenile polyposis
syndrome · Familial adenomatous polyposis/Gardner's syndrome ·
Colon/rectum Cronkhite–Canada disease
neoplasm: Adenocarcinoma · Familial adenomatous polyposis ·
Hereditary nonpolyposis colorectal cancer

Anus Squamous cell carcinoma

Upper
and/or Gastrointestinal stromal tumor · Krukenberg tumor (metastatic)
lower

malignant: Hepatocellular carcinoma (Fibrolamellar) · Hepatoblastoma

ALiver benign: Hepatocellular adenoma · Cavernous hemangioma
c
hyperplasia: Focal nodular hyperplasia · Nodular regenerative hyperplasia
c
e
sBiliary bile duct: Cholangiocarcinoma · Klatskin tumor
stract gallbladder: Gallbladder cancer
o
r exocrine pancreas: Adenocarcinoma · Pancreatic ductal carcinoma
yPancreascystic neoplasms: Serous microcystic adenoma · Intraductal papillary mucinous
neoplasm · Mucinous cystic neoplasm · Solid pseudopapillary neoplasm
Pancreatoblastoma

P
e
r
i
tPrimary peritoneal carcinoma · Peritoneal mesothelioma · Desmoplastic small round cell
otumor
n
e
u
m

M: DIG anat(t, g, noco/cong/tumr, proc,

p)/phys/devp/cell/enzy sysi/epon drug(A2A/2B/3/4/5/6/7/14/16),
blte

[show]
v•d•e
Tumors: Mediastinal tumors/Thoracic neoplasm/respiratory neoplasia (C30-
C34/D14, 160-163/212.0-212.4)

Unasal cavity: Esthesioneuroblastoma

p
pnasopharynx: Nasopharyngeal carcinoma · Nasopharyngeal angiofibroma
e
r
larynx: Laryngeal cancer · Laryngeal papillomatosis
R
T

TracheaTracheal tumor

Non-
Squamous cell carcinoma · Adenocarcinoma of the lung · Large cell
small cell
L lung carcinoma · Sarcomatoid carcinoma · Carcinoid · Salivary
lung
o gland-like carcinoma · Adenosquamous carcinoma
carcinoma
w
e
Small cell
r Combined small cell carcinoma
Lung carcinoma
R
T Non-
Sarcoma · Lymphoma · Immature teratoma · Melanoma
carcinoma

By
Pancoast tumor · Solitary pulmonary nodule
location

P
l
e
Mesothelioma · Malignant solitary fibrous tumor
u
r
a

M: RES anat(n, x, l, noco(c)/cong/tumr, proc,

c)/phys/devp sysi/epon, injr drug(R1/2/3/5/6/7)

[show]
v•d•e
Tumors: Mediastinal tumor: Thymus neoplasia (C37/D15.0, 164.0/212.6)

A
&
Thymoma
B

C
Thymus

M: LMO anat(h, u, t, a, l)/phys lydi/spdi/thdi/thtu/vatu proc

[show]
v•d•e
Tumors: Mediastinal tumor: Heart neoplasia (C38.0/D15.1, 164.1/212.7)

C
Myxoma (Atrial myxoma)
o
n
n
e
c
t
i
v
e

t
i
s
s
u
e

n
e
o
p
l
a
s
m

O
t
h
e
r

PPapillary fibroelastoma · Rhabdomyoma · Lipoma · Angiosarcoma · Teratoma

r
i
m
a
r
y

O
t
hSecondary
e
r

M: HRT anat/phys/devp noco/cong/tumr, proc, drug

sysi/epon (C1A/1B/1C/1D), blte

[show]
v•d•e
 Connective tissue neoplasm: Osseous and Chondromatous tumors (ICD-O
9180-9269) (C40-C41/D16, 170/213)

D
i
aMyeloid Multiple myeloma
p
hEpithelial Adamantinoma
y
sPNET/Ewing
Ewing's sarcoma
ifamily
s

Osteoid osteoma · Osteoblastoma

MOsteoblast
e Osteoma/osteosarcoma
t
a Chondroma/ecchondroma/enchondroma (Enchondromatosis, Extraskeletal
p chondroma) · Chondrosarcoma (Mesenchymal chondrosarcoma, Myxoid
hChondroblastchondrosarcoma)
y
s Osteochondroma (Osteochondromatosis)
i Chondromyxoid fibroma
s
Fibrous Ossifying fibroma · Fibrosarcoma

EChondroblastChondroblastoma
p
iMyeloid Giant cell tumor of bone
p
h
y
s
i
s

O
NotochordChordoma
t
h
e
r
/
u
n
g
r
o
u
p
e
d
 M: BON/CAR anat(c/f/k/f, u, t/p, noco/cong/tumr, proc, drug(M5)
l)/phys/devp/cell sysi/epon, injr

[show]
v•d•e
Tumors: Skin neoplasm, Nevi and melanomas (C43/D22, 172/216)

M
eMucosal melanoma · Superficial spreading melanoma · Nodular melanoma · lentigo
l(Lentigo maligna/Lentigo maligna melanoma, Acral lentiginous melanoma)
aAmelanotic melanoma · Desmoplastic melanoma · Melanoma with features of a Spitz
nnevus · Melanoma with small nevus-like cells · Polypoid melanoma · Soft-tissue
omelanoma
m
aMelanocytic tumors of uncertain malignant potential

N
e
v
u
s
/

m
eNevus of Ito · Nevus of Ota · Compound nevus · Spitz nevus · Halo nevus ·
lPseudomelanoma · Blue nevus (Blue nevus of Jadassohn–Tièche, Cellular blue nevus,
aEpithelioid blue nevus, Deep penetrating nevus, Amelanotic blue nevus, Malignant blue
nnevus) · Giant pigmented nevus · Congenital melanocytic nevus (Medium-sized
ocongenital nevocytic nevus, Small-sized congenital nevocytic nevus) · Balloon cell
cnevus · Dysplastic nevus/Dysplastic nevus syndrome
yAcral nevus · Becker's nevus · Benign melanocytic nevus · Nevus spilus · Pigmented
tspindle cell nevus
i
c

n
e
v
u
s

Plentigo/lentiginosis: Centrofacial lentiginosis · Generalized lentiginosis · Inherited

ipatterned lentiginosis in black persons · Ink spot lentigo · Lentigo maligna · Lentigo
gsimplex · Mucosal lentigines · Partial unilateral lentiginosis · PUVA lentigines · Solar
mlentigo
e
nEphelis · Melanoacanthoma
t
a
t
i
o
n

d
i
s
o
r
d
e
r

S
y
n
d
rCarney complex · Moynahan syndrome · Peutz–Jeghers syndrome
o
m
e
s

M: INT, anat/phys/devp noco(i,b,d,q,u,r,p,k,c,v)/cong/tumr(n,e,d), proc, drug

SF, LCT sysi/epon (D2/3/4/5/8)

[show]
v•d•e
Connective/soft tissue tumors and sarcomas (ICD-O 8800-9059) (C45-
C49/D17-D21, 171/214-215)

N
Soft tissue sarcoma · Desmoplastic small round cell tumor
o
t

o
t
h
e
r
w
i
s
e

s
p
e
c
i
f
i
e
d

(
8
8
0
0
-
8
8
0
9
)

C Fibroma/fibrosarcoma: Dermatofibrosarcoma · Dermatofibrosarcoma

o protuberans · Desmoplastic fibroma
n
n Fibroma/fibromatosis: Aggressive infantile fibromatosis · Aponeurotic
e fibroma · Collagenous fibroma · Diffuse infantile fibromatosis · Familial
cFibromatous myxovascular fibromas · Fibroma of tendon sheath · Fibromatosis colli ·
t(8810-8839) Infantile digital fibromatosis · Juvenile hyaline fibromatosis · Plantar
i fibromatosis · Pleomorphic fibroma · Oral submucous fibrosis
v Histiocytoma/histiocytic sarcoma: Benign fibrous histiocytoma ·
e Malignant fibrous histiocytoma · Atypical fibroxanthoma

t Solitary fibrous tumor

i
sMyxomatous Myxoma/myxosarcoma (Cutaneous myxoma, Superficial acral
s(8840-8849) fibromyxoma) · Angiomyxoma · Ossifying fibromyxoid tumour
u
eFibroepithelial Brenner tumour · Fibroadenoma · Phyllodes tumor
(9000-9039)
n
eSynovial-like Synovial sarcoma · Clear-cell sarcoma
o(9040-9049)
p
l
a
s
m

LLipoma/liposarcoma (Myelolipoma, Myxoid liposarcoma) · PEComa

i(Angiomyolipoma)
p
oChondroid lipoma · Intradermal spindle cell lipoma · Pleomorphic lipoma · Benign
mlipoblastomatosis · Spindle cell lipoma · Hibernoma
a
t
o
u
s

(
8
8
5
0
-
8
8
8
9
)

M
y
o
m
a
t
ogeneral: Myoma/myosarcoma
usmooth muscle: Leiomyoma/leiomyosarcoma
s
skeletal muscle: Rhabdomyoma/rhabdomyosarcoma: Embryonal rhabdomyosarcoma
((Sarcoma botryoides) · Alveolar rhabdomyosarcoma
8
8Leiomyoma · Angioleiomyoma · Angiolipoleiomyoma · Genital leiomyoma ·
9Leiomyosarcoma · Multiple cutaneous and uterine leiomyomatosis syndrome · Multiple
0cutaneous leiomyoma · Neural fibrolipoma · Solitary cutaneous leiomyoma
-
8
9
2
9
)

CAdenomyoma · Pleomorphic adenoma · Mixed Müllerian tumor · Mesoblastic

onephroma · Wilms' tumor · Rhabdoid tumour · Clear-cell sarcoma of the kidney ·
mHepatoblastoma · Pancreatoblastoma · Carcinosarcoma
p
l
e
x

m
i
x
e
d
a
n
d

s
t
r
o
m
a
l

(
8
9
3
0
-
8
9
9
9
)

M
e
s
o
t
h
e
l
i
a
l
Mesothelioma · Adenomatoid tumor
(
9
0
5
0
-
9
0
5
9
)

M: MUS, DF+DRCT anat (h/n, u, t/d, a/p, noco(m, s, proc, drug (M1A/3)
l)/phys/hist c)/cong(d)/tumr,
sysi/epon, injr
 [show]
v•d•e
Vascular tissue neoplasm (ICD-O 9120-9179) (C49+C46/D18, 171+176/215)

Hemangioma/hemangiosarcoma · Blue rubber bleb nevus syndrome ·

Hemangioendothelioma (Infantile hemangioendothelioma · Endovascular papillary
hemangioendothelioma · Epithelioid hemangioendothelioma · Spindle cell
hemangioendothelioma · Composite hemangioendothelioma · Proliferating
angioendotheliomatosis · Retiform hemangioendothelioma) · Hemangiopericytoma ·
BAngiokeratoma · Capillary hemangioma (Hemangioblastoma) · Cavernous
lhemangioma · Venous lake
o
Kaposi's sarcoma: African cutaneous Kaposi sarcoma · African lymphadenopathic
o
Kaposi sarcoma · AIDS-associated Kaposi sarcoma · Classic Kaposi sarcoma ·
d
Immunosuppression-associated Kaposi sarcoma · Kaposiform hemangioendothelioma
Angioma serpiginosum · Cherry angioma · Glomeruloid hemangioma · Microvenular
hemangioma · Spider angioma · Targetoid hemosiderotic hemangioma · Tufted
angioma · Universal angiomatosis
Angiokeratoma · Angiokeratoma of Mibelli · Angiolipoma

L
y
m
Lymphangioma/lymphangiosarcoma · PEComa (Lymphangioleiomyomatosis) · Cystic
p
hygroma · Lymphangioma circumscriptum
h
aMultifocal lymphangioendotheliomatosis · Acquired progressive lymphangioma ·
tLymphangiomatosis
i
c

E
i
t
Angioma/angiosarcoma · Angiofibroma
h
e
r

M: anat(a:h,u,t,a,l,v:h,u,t,a,l)/phys/devp/c noco/syva/cong/tu proc,

VA ell/prot mr, sysi/epon drug(C2s/n,C3,C4,C5,C7,C
S 8,C9)

M: LMO anat(h, u, t, a, l)/phys lydi/spdi/thdi/thtu/vatu proc

[show]
v•d•e
Tumors: breast cancer (C50/D24, 174-175/217) - Histopathologic
classification
F
i
b
r
o
e
p
i
t
h
e
lPhyllodes tumor
i
a
l
/
s
t
r
o
m
a
l

D Ductal carcinoma in situ (DCIS): Paget's disease of the breast ·

u Comedocarcinoma
cDuctal
t Invasive ductal carcinoma (IDC)
a Intraductal papilloma
l
,
Lobular carcinoma in situ (LCIS)
Lobular
l Invasive lobular carcinoma (ILC)
o
bMedullary Medullary carcinoma
u
lOther/ungroupedInflammatory breast cancer
a
r
,

a
n
d

m
e
d
u
l
l
a
r
y

P
r
e
c
u
r
s
o
rAtypical ductal hyperplasia

l
e
s
i
o
n
s

O
t
hNipple adenoma
e
r

M: BRE anat/phys noco/cong/tumr proc

[show]
v•d•e
Tumors: female urogenital neoplasia · (C51-C58/D25-28, 179-184/218-221)

A Glandular
d and
n CMS: Ovarian serous cystadenoma · Mucinous cystadenoma ·
epithelial/
e Cystadenocarcinoma (Papillary serous cystadenocarcinoma) ·
surface
x Krukenberg tumor
epithelial-
a stromal Endometrioid tumor · Clear-cell ovarian carcinoma · Brenner tumour
tumor

Ovaries Sex cord-

Leydig cell tumour · Sertoli cell tumour · Sertoli-Leydig cell
gonadal
tumour · Thecoma · Granulosa cell tumour · Luteoma
stromal

Dysgerminoma · Nongerminomatous (Embryonal carcinoma,

Germ cell Endodermal sinus tumor, Gonadoblastoma, Teratoma/Struma ovarii,
Choriocarcinoma)

Fibroma Meigs syndrome

Fallopian
Adenomatoid tumor
tube

Myometrium Uterine fibroids/leiomyoma · Leiomyosarcoma · Adenomyoma

U Endometrioid tumor · Uterine papillary serous carcinoma · Clear cell

Endometrium
t carcinoma · Endometrial intraepithelial neoplasia
e
rCervix SCC · Cervical intraepithelial neoplasia
u
sPlacenta Choriocarcinoma · Gestational trophoblastic disease

General Uterine sarcoma · Mixed Müllerian tumor

V
a
gSCC · Botryoid rhabdomyosarcoma · Clear cell adenocarcinoma of the vagina · Vaginal
iintraepithelial neoplasia
n
a

V
u
SCC · Melanoma · Papillary hidradenoma · Extramammary Paget's disease · Vulvar
l
intraepithelial neoplasia
v
a

M: ♀ FRS anat/phys/devp noco/cong/npls, proc/asst, drug

sysi/epon (G1/G2B/G3CD)

[show]
v•d•e
Tumors: male urogenital neoplasia · genital neoplasia (C60-C63/D29, 185-
187/222)

Sex
cord-
Sertoli-Leydig cell tumour (Sertoli cell tumor, Leydig cell tumor)
gonadal
I stromal
n
tTesticles
Seminoma (Spermatocytic seminoma) · Intratubular germ cell
e G
neoplasia
r Germ
n cell
Embryonal carcinoma · Endodermal sinus tumor ·
a NG
Gonadoblastoma · Teratoma · Choriocarcinoma · Embryoma
l
Adenocarcinoma · Prostatic intraepithelial neoplasia (HGPIN) · Small cell
Prostate
carcinoma · Transitional cell carcinoma
E Carcinoma (Extramammary Paget's disease) · Bowen's disease · Bowenoid
xPenispapulosis · Erythroplasia of Queyrat · Hirsuties papillaris genitalis
t
e
r
n
a
l

M: ♂ MRS anat/phys/devp noco/cong/tumr, proc, drug

sysi/epon (G3B/4B/4C)

[show]
v•d•e
Tumors: urogenital neoplasia: urinary organs (C64-C68/D30, 188-189/223)

A Glandular and epithelial neoplasm: Renal cell carcinoma · Renal oncocytoma

b
d Complex and mixed tumor: Wilms' tumor · Mesoblastic nephroma · Clear-cell
oKidney sarcoma of the kidney · Angiomyolipoma · Cystic nephroma · Metanephric
m adenoma
i by location: Renal medullary carcinoma · Juxtaglomerular cell tumor
n
aUreter Ureteral neoplasm
l

PBladderTransitional cell carcinoma · Inverted papilloma · Squamous cell carcinoma

e
l Transitional cell carcinoma · Squamous cell carcinoma · Adenocarcinoma ·
vUrethra Melanoma
i
c

R
e
t
r
o
p
e
rMalignant fibrous histiocytoma
i
t
o
n
e
u
m

M: URI anat/phys/devp/cell noco/acba/cong/tumr, proc/itvp, drug

 sysi/epon, urte (G4B), blte, urte

[show]
v•d•e
Eye neoplasm (C69/D31, 190/224)

M
e
l
a
Uveal melanoma · Ciliary body melanoma
n
o
m
a

O
t
hRetinoblastoma · Medulloepithelioma/Diktyoma
e
r

M: EYE anat(g, a, noco/cong/tumr, epon proc,

p)/phys/devp/cell/prot drug(S1A/1E/1F/1L)

[show]
v•d•e
Nervous tissue tumors/NS neoplasm/Neuroectodermal tumor (ICD-O 9350-
9589) (C70-C72/D32-D33, 191-192/225)

Esellar: Craniopharyngioma · Pituicytoma

n
dother: Pinealoma
o
c
r
i
n
e
/

s
e
l
l
a
r

(
9
3
5
0
-
9
3
7
9
)

Astrocytoma (Pilocytic astrocytoma,

Pleomorphic xanthoastrocytoma, Fibrillary
Astrocyte (also diffuse or lowgrade) astrocytomas,
Anaplastic astrocytoma, Glioblastoma
multiforme)

Oligodendrocyte Oligodendroglioma
Glioma
C Ependyma Ependymoma · Subependymoma
N
S Choroid plexus tumor (Choroid plexus
Choroid plexus
Neuroepithelial papilloma, Choroid plexus carcinoma)
((brain tumors,
9spinal tumors)
Oligoastrocytoma · Gliomatosis cerebri ·
3 Multiple/unknown
Gliosarcoma
8
0
- Ganglioneuroma: Ganglioglioma · Retinoblastoma ·
Mature
9 Neurocytoma · Dysembryoplastic neuroepithelial tumour ·
neuron
5 Lhermitte-Duclos disease
3
9 Neuroblastoma (Esthesioneuroblastoma,
) PNET Ganglioneuroblastoma) · Medulloblastoma · Atypical teratoid
rhabdoid tumor

PrimitiveMedulloepithelioma

Meningiomas
Meningioma
(meninges)

Hematopoietic Primary central nervous system lymphoma

Pcranial and paraspinal nerves: Neurofibroma (Neurofibrosarcoma, Neurofibromatosis) ·

NNeurilemmoma/Schwannoma (Acoustic neuroma) · Malignant peripheral nerve sheath
Stumor
:

N
S
T

(
9
5
4
0
-
9
5
7
9
)

note: not all brain tumors are of nervous tissue, and not all nervous tissue tumors are in
the brain (see brain metastases)
M: anat(s,m,p,4,e,b,d,c,a,f,l,g)/p noco(m,d,e,h,v,s)/cong/tumr, proc,drug(N1A/2AB/C/3/4
C hys/devp/cell sysi/epon,injr /7A/B/C/D)
NS

M: anat(h,r,t,c,b,l,s)/phys/devp/prot/nttr/nttm/ntrp noco/auto/cong/tumr, proc,

PNS sysi/epon, injr drug(N1B)

[show]
v•d•e
Tumors: endocrine gland neoplasia (C73-C75/D34-D35, 193-194/226-227)

Pneuroendocrine tumors/islet cell carcinoma: α:Glucagonoma · β:Insulinoma ·

aδ:Somatostatinoma · G:Gastrinoma · VIPoma
n
c
r
e
a
s
/

i
s
l
e
t
s

o
f

L
a
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r
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H Pituitary adenoma: Prolactinoma · ACTH-secreting pituitary adenoma · GH-

y secreting pituitary adenoma
pPituitary
o Craniopharyngioma
t Pituicytoma
h
a
l Thyroid cancer (malignant): epithelial cell /carcinoma (Papillary,
aThyroid Follicular/Hurthle cell) · parafollicular cell (Medullary) · Anaplastic
m Benign: Thyroid adenoma · Struma ovarii
i
cParathyroidParathyroid adenoma · Parathyroid carcinoma
/
adrenal cortex (Adrenocortical adenoma, Adrenocortical carcinoma)
pAdrenal
itumor adrenal medulla (Pheochromocytoma, Neuroblastoma) · see also
t Paraganglioma
u
iGonads see genital neoplasia
t
a
r
y

a
x
e
s

+
p
a
r
a
t
h
y
r
o
i
d

PPinealoblastoma · Pineocytoma
i
n
e
a
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o
m
a

M
E
1 · 2A · 2B
N

M: END anat/phys/devp/horm/cell noco(d)/cong/tumr, proc, drug

sysi/epon (A10/H1/H2/H3/H5)

[show]
v•d•e
Hematological malignancy/leukemia histology (ICD-O 9590-9989, C81-C96,
200-208)
Lymphoid/Lymphoproliferative, Lymphomas/Lymphoid leukemias (9590-
9739, 9800-9839)

B cell ALL (Precursor B acute

(lymphoma, TdT+
lymphoblastic leukemia/lymphoma)
leukemia)
(most CD19,
naive B cell (CLL/SLL)
CD20) CD5+
mantle zone (Mantle cell)

Prolymphocytic · CD11c (Hairy cell

CD22+
leukemia)

By germinal center/follicular B cell

development/ (Follicular, Burkitt's, GCB-DLBCL)
marker CD79a+ marginal zone/marginal-zone B cell
(Splenic marginal zone, MALT,
Nodal marginal zone)

Classic Hodgkin's lymphoma

RS (CD15+, (Nodular sclerosis) · CD20 (Nodular
CD30+) lymphocyte predominant Hodgkin's
lymphoma)

PCDs/PP see immunoproliferative

(CD38+/CD138+) immunoglobulin disorders

KSHV (Primary effusion) · EBV (Lymphomatoid

granulomatosis, Post-transplant lymphoproliferative
By infection
disorder) · HIV (AIDS-related lymphoma) ·
Helicobacter pylori (MALT lymphoma)

Ungrouped Diffuse large B-cell lymphoma • Intravascular large B-

 cell lymphoma • Primary cutaneous marginal zone
lymphoma • Primary cutaneous immunocytoma •
Plasmacytoma • Plasmacytosis

TdT+: ALL (Precursor T acute

lymphoblastic leukemia/lymphoma)
By development/
marker prolymphocyte (Prolymphocytic)
CD30+ (Anaplastic large cell,
T cell
Lymphomatoid papulosis)
(lymphoma,
leukemia)
(most CD3, Cutaneous (Mycosis fungoides,
CD4, CD8) By Sézary's disease) · Hepatosplenic ·
location/peripheral Angioimmunoblastic · Enteropathy-
associated T-cell lymphoma

HTLV-1 (Adult T-cell

By infection
leukemia/lymphoma)
T/NK
NK cell/
Aggressive NK-cell leukemia · Blastic NK cell
(most
lymphoma
CD56)

EBV (Extranodal NK-T-cell lymphoma) · Large granular

T or NK
lymphocytic leukemia

CD30+ cutaneous T-cell lymphoma •

Angioimmunoblastic T-cell lymphoma • Subcutaneous
T-cell lymphoma • Non-mycosis fungoides CD30−
Ungrouped
cutaneous large T-cell lymphoma • Pleomorphic T-cell
lymphoma • Lennert lymphoma • Secondary cutaneous
CD30+ large cell lymphoma • Angiocentric lymphoma

Lymphoid+myeloi
Acute biphenotypic leukaemia
d

Lymphoproliferative disorders (X-linked lymphoproliferative

disease, Autoimmune lymphoproliferative syndrome) · Leukemoid
Lymphocytosis
reaction · Pseudolymphoma · Diffuse infiltrative lymphocytosis
syndrome

UCutaneous lymphoid hyperplasia • Cutaneous lymphoid hyperplasia with bandlike and

nperivascular patterns • Cutaneous lymphoid hyperplasia with nodular pattern • Jessner
glymphocytic infiltrate of the skin
r
oGranulomatous slack skin • Kikuchi disease • Leukemia cutis • Lymphomatoid
upapulosis • Leukemid • Pagetoid reticulosis • Primary cutaneous follicular lymphoma •
pSinus histiocytosis with massive lymphadenopathy
e
d
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y
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M: LMC cell/phys/auag/auab/comp,imrc,tcrp imdf/ipig/hyps/tumr proc, drug(L3/4)

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ICD-10 Chapter III: Diseases of the blood

and blood-forming organs, and certain
disorders involving the immune
mechanism
From Wikipedia, the free encyclopedia
Jump to: navigation, search
International Statistical Classification of Diseases and Related Health Problems 10th
Revision
Chapter Blocks Title
I A00-B99 Certain infectious and parasitic diseases
II C00-D48 Neoplasms
D50- Diseases of the blood and blood-forming organs and certain disorders
III
D89 involving the immune mechanism
IV E00-E90 Endocrine, nutritional and metabolic diseases
V F00-F99 Mental and behavioural disorders
G00-
VI Diseases of the nervous system
G99
H00-
VII Diseases of the eye and adnexa
H59
H60-
VIII Diseases of the ear and mastoid process
H95
IX I00-I99 Diseases of the circulatory system
X J00-J99 Diseases of the respiratory system
K00-
XI Diseases of the digestive system
K93
XII L00-L99 Diseases of the skin and subcutaneous tissue
M00-
XIII Diseases of the musculoskeletal system and connective tissue
M99
N00-
XIV Diseases of the genitourinary system
N99
O00-
XV Pregnancy, childbirth and the puerperium
O99
XVI P00-P96 Certain conditions originating in the perinatal period
Q00- Congenital malformations, deformations and chromosomal
XVII
Q99 abnormalities
Symptoms, signs and abnormal clinical and laboratory findings, not
XVIII R00-R99
elsewhere classified
XIX S00-T98 Injury, poisoning and certain other consequences of external causes
V01-
XX External causes of morbidity and mortality
Y98
XXI Z00-Z99 Factors influencing health status and contact with health services
U00-
XXII Codes for special purposes
U99
The International Statistical Classification of Diseases and Related Health Problems 10th
Revision (ICD-10) is a coding of diseases and signs, symptoms, abnormal findings,
complaints, social circumstances and external causes of injury or diseases, as classified
by the World Health Organization (WHO).[1]. This page contains ICD-10 Chapter III:
Diseases of the blood and blood-forming organs, and certain disorders involving the
immune mechanism.

Contents
[hide]
• 1 D50-D89 - Diseases of the blood and blood-forming organs and certain
 disorders involving the immune mechanism
○ 1.1 (D50-D53) Nutritional anemias
○ 1.2 (D55-D59) Haemolytic anaemias
○ 1.3 (D60-D64) Aplastic and other anaemias
○ 1.4 (D65-D69) Coagulation defects, purpura and other haemorrhagic
conditions
○ 1.5 (D70-D77) Other diseases of blood and blood-forming organs
○ 1.6 (D80-D89) Certain disorders involving the immune mechanism
• 2 See also
• 3 References

[edit] D50-D89 - Diseases of the blood and blood-

forming organs and certain disorders involving the
immune mechanism
[edit] (D50-D53) Nutritional anemias
• (D50.) Iron deficiency anaemia
○ (D50.0) Iron deficiency anaemia secondary to blood loss (chronic)
○ (D50.1) Sideropenic dysphagia
 Kelly-Paterson syndrome
 Plummer-Vinson syndrome
○ (D50.8) Other iron deficiency anaemias
○ (D50.9) Iron deficiency anaemia, unspecified
• (D51.) Vitamin B12 deficiency anaemia
○ (D51.0) Vitamin B12 deficiency anaemia due to intrinsic factor deficiency
 Pernicious anemia
○ (D51.1) Vitamin B 12 deficiency anaemia due to selective vitamin B 12
malabsorption with proteinuria
 Megaloblastic hereditary anaemia
○ (D51.2) Transcobalamin II deficiency
○ (D51.3) Other dietary vitamin B 12 deficiency anaemia
○ (D51.8) Other vitamin B 12 deficiency anaemias
○ (D51.9) Vitamin B 12 deficiency anaemia, unspecified
• (D52.) Folate deficiency anaemia
○ (D52.0) Dietary folate deficiency anaemia
 Nutritional megaloblastic anaemia
○ (D52.1) Drug-induced folate deficiency anaemia
○ (D52.8) Other folate deficiency anaemias
 ○ (D52.9) Folate deficiency anaemia, unspecified
• (D53.) Other nutritional anaemias
○ (D53.0) Protein deficiency anaemia
○ (D53.1) Other megaloblastic anaemias, not elsewhere classified
○ (D53.2) Scorbutic anaemia
○ (D53.8) Other specified nutritional anaemias
○ (D53.9) Nutritional anaemia, unspecified
[edit] (D55-D59) Haemolytic anaemias
• (D55.) Anaemia due to enzyme disorders
○ (D55.0) Anaemia due to glucose-6-phosphate dehydrogenase (G6PD)
deficiency
 Favism
 G6PD deficiency anaemia
○ (D55.1) Anaemia due to other disorders of glutathione metabolism
○ (D55.2) Anaemia due to disorders of glycolytic enzymes
 hexokinase deficiency
 pyruvate kinase deficiency
 triose-phosphate isomerase deficiency
○ (D55.3) Anaemia due to disorders of nucleotide metabolism
○ (D55.8) Other anaemias due to enzyme disorders
○ (D55.9) Anaemia due to enzyme disorder, unspecified
• (D56.) Thalassaemia
○ (D56.0) Alpha thalassaemia
○ (D56.1) Beta thalassaemia
○ (D56.2) Delta-beta thalassaemia
○ (D56.3) Thalassaemia trait
○ (D56.4) Hereditary persistence of fetal haemoglobin (HPFH)
○ (D56.8) Other thalassaemias
○ (D56.9) Thalassaemia, unspecified
• (D57.) Sickle-cell disorders
○ (D57.0) Sickle-cell anaemia with crisis
○ (D57.1) Sickle-cell anaemia without crisis
○ (D57.2) Double heterozygous sickling disorders
○ (D57.3) Sickle-cell trait
○ (D57.8) Other sickle-cell disorders
• (D58.) Other hereditary haemolytic anaemias
○ (D58.0) Hereditary spherocytosis
  Acholuric (familial) jaundice
 Congenital (spherocytic) haemolytic icterus
 Minkowski-Chauffard syndrome
○ (D58.1) Hereditary elliptocytosis
 Elliptocytosis (congenital)
 Ovalocytosis (congenital)(hereditary)
○ (D58.2) Other haemoglobinopathies
 Abnormal haemoglobin NOS
 Congenital Heinz body anaemia
 Haemoglobinopathy NOS
 Unstable haemoglobin haemolytic disease
○ (D58.8) Other specified hereditary haemolytic anaemias
 Stomatocytosis
• (D59.) Acquired haemolytic anaemia
○ (D59.0) Drug-induced autoimmune haemolytic anaemia
○ (D59.1) Other autoimmune haemolytic anaemias
 Warm autoimmune hemolytic anemia
○ (D59.2) Drug-induce nonautoimmune haemolytic anaemia
○ (D59.3) Haemolytic-uraemic syndrome
○ (D59.4) Other nonautoimmune haemolytic anaemias
 Microangiopathic hemolytic anemia
○ (D59.5) Paroxysmal nocturnal haemoglobinuria (Marchiafava-Micheli)
○ (D59.6) Haemoglobinuria due to haemolysis from other external causes
 paroxysmal cold haemoglobinuria
○ (D59.8) Other acquired haemolytic anaemias
○ (D59.9) Acquired haemolytic anaemia, unspecified
[edit] (D60-D64) Aplastic and other anaemias
• (D60.) Acquired pure red cell aplasia (erythroblastopenia)
• (D61.) Other aplastic anaemias
○ (D61.0) Constitutional aplastic anaemia
 Blackfan-Diamond syndrome
 Familial hypoplastic anaemia
 Fanconi's anaemia
 Pancytopenia with malformations
○ (D61.1) Drug-induced aplastic anaemia
○ (D61.2) Aplastic anaemia due to other external agents
○ (D61.3) Idiopathic aplastic anaemia
 ○ (D61.8) Other specified aplastic anaemias
○ (D61.9) Aplastic anaemia, unspecified
 Hypoplastic anaemia NOS
 Medullary hypoplasia
 Panmyelophthisis
• (D62.) Acute posthaemorrhagic anaemia
• (D63.) Anaemia in chronic diseases classified elsewhere
• (D64.) Other anaemias
○ (D64.0) Hereditary sideroblastic anaemia
○ (D64.1) Secondary sideroblastic anaemia due to disease
○ (D64.2) Secondary sideroblastic anaemia due to drugs and toxins
○ (D64.3) Other sideroblastic anaemias
○ (D64.4) Congenital dyserythropoietic anaemia
○ (D64.8) Other specified anaemias
○ (D64.9) Anaemia, unspecified
[edit] (D65-D69) Coagulation defects, purpura and other haemorrhagic
conditions
• (D65.) Disseminated intravascular coagulation (defibrination syndrome)
○ Afibrinogenaemia, acquired
○ Consumption coagulopathy
○ Diffuse or disseminated intravascular coagulation (DIC)
○ Fibrinolytic haemorrhage, acquired
○ Fibrinolytic purpura
○ Purpura fulminans
• (D66.) Hereditary factor VIII deficiency
○ Haemophilia A
• (D67.) Hereditary factor IX deficiency
○ Christmas disease
○ Haemophilia B
• (D68.) Other coagulation defects
○ (D68.0) Von Willebrand's disease
○ (D68.1) Hereditary factor XI deficiency
 Haemophilia C
○ (D68.2) Hereditary deficiency of other clotting factors
○ (D68.3) Haemorrhagic disorder due to circulating anticoagulants
○ (D68.4) Acquired coagulation factor deficiency
○ (D68.8) Other specified coagulation defects
 ○ (D68.9) Coagulation defect, unspecified
• (D69.) Purpura and other haemorrhagic conditions
○ (D69.0) Allergic purpura
 anaphylactoid purpura
 Henoch-Schönlein purpura
○ (D69.1) Qualitative platelet defects
 Bernard-Soulier syndrome (giant platelet)
 Glanzmann's disease
 Grey platelet syndrome
 Thromboasthenia (haemorrhagic)(hereditary)
 Thrombocytopathy
○ (D69.2) Other nonthrombocytopenic purpura
○ (D69.3) Idiopathic thrombocytopenic purpura
 Evans' syndrome
○ (D69.4) Other primary thrombocytopenia
○ (D69.5) Secondary thrombocytopenia
○ (D69.6) Thrombocytopenia, unspecified
○ (D69.8) Other specified haemorrhagic conditions
○ (D69.9) Haemorrhagic condition, unspecified
[edit] (D70-D77) Other diseases of blood and blood-forming organs
• (D70.) Agranulocytosis
○ Agranulocytic angina
○ Infantile genetic agranulocytosis
○ Kostmann's disease
○ Neutropenia, NOS
• (D71.) Functional disorders of polymorphonuclear neutrophils
○ Cell membrane receptor complex (CR3) defect
○ Chronic (childhood) granulomatous disease
○ Congenital dysphagocytosis
○ Progressive septic granulomatosis
• (D72.) Other disorders of white blood cells
○ (D72.0) Genetic anomalies of leukocytes
 Alder anomaly
 May-Hegglin anomaly
 Pelger-Huët anomaly
○ (D72.1) Eosinophilia
○ (D72.8) Other specified disorders of white blood cells
  Leukaemoid reaction: lymphocytic, monocytic, myelocytic
 Leukocytosis
 Lymphocytosis (symptomatic)
 Lymphopenia
 Monocytosis (symptomatic)
 Plasmacytosis
○ (D72.9) Disorder of white blood cells, unspecified
• (D73.) Diseases of spleen
○ (D73.0) Hyposplenism
○ (D73.1) Hypersplenism
○ (D73.2) Chronic congestive splenomegaly
○ (D73.3) Abscess of spleen
○ (D73.4) Cyst of spleen
○ (D73.5) Infarction of spleen
○ (D73.8) Other diseases of spleen
○ (D73.9) Disease of spleen, unspecified
• (D74.) Methaemoglobinaemia
○ (D74.0) Congenital methaemoglobinaemia
 Congenital NADH-methaemoglobin reductase deficiency
 Haemoglobin-M (Hb-M) disease
 Methaemoglobinaemia, hereditary
○ (D74.8) Other methaemoglobinaemias
 Acquired methaemoglobinaemia (with sulfhaemoglobinaemia)
 Toxic methaemoglobinaemia
○ (D74.9) Methaemoglobinaemia, unspecified
• (D75.) Other diseases of blood and blood-forming organs
○ (D75.0) Familial erythrocytosis
○ (D75.1) Secondary polycythaemia
○ (D75.2) Essential thrombocytosis
○ (D75.8) Other specified diseases of blood and blood-forming organs
 Basophilia
○ (D75.9) Disease of blood and blood-forming organs, unspecified
• (D76.) Certain diseases involving lymphoreticular tissue and reticulohistiocytic
system
○ (D76.0) Langerhans' cell histiocytosis, not elsewhere classified
 Eosinophilic granuloma
 Hand-Schüller-Christian disease
  Histiocytosis X (chronic)
○ (D76.1) Haemophagocytic lymphohistiocytosis
 Familial haemophagocytic reticulosis
○ (D76.2) Haemophagocytic syndrome, infection-associated
○ (D76.3) Other histiocytosis syndromes
 Reticulohistiocytoma (giant-cell)
 Sinus histiocytosis with massive lymphadenopathy
 Xanthogranuloma
• (D77.) Other disorders of blood and blood-forming organs in diseases classified
elsewhere
[edit] (D80-D89) Certain disorders involving the immune mechanism
• (D80.) Immunodeficiency with predominantly antibody defects
○ (D80.0) Hereditary hypogammaglobulinaemia
 Autosomal recessive agammaglobulinaemia (Swiss type)
 X-linked agammaglobulinaemia (Bruton) (with growth hormone
deficiency)
○ (D80.1) Nonfamilial hypogammaglobulinaemia
 Agammaglobulinaemia with immunoglobulin-bearing B-
lymphocytes
 Common variable agammaglobulinaemia (CVAgamma)
 Hypogammaglobulinaemia NOS
○ (D80.2) Selective deficiency of immunoglobulin A (IgA)
○ (D80.3) Selective deficiency of immunoglobulin G (IgG) subclasses
○ (D80.4) Selective deficiency of immunoglobulin M (IgM)
○ (D80.5) Immunodeficiency with increased immunoglobulin M (IgM)
○ (D80.6) Antibody deficiency with near-normal immunoglobulins or with
hyperimmunoglobulinaemia
○ (D80.7) Transient hypogammaglobulinaemia of infancy
○ (D80.8) Other immunodeficiencies with predominantly antibody defects
 Kappa light chain deficiency
○ (D80.8) Immunodeficiency with predominantly antibody defects,
unspecified
• (D81.) Combined immunodeficiencies
○ (D81.0) Severe combined immunodeficiency (SCID) with reticular
dysgenesis
○ (D81.1) Severe combined immunodeficiency (SCID) with low T-cell and
B-cell numbers
○ (D81.2) Severe combined immunodeficiency (SCID) with low or normal
B-cell numbers
 ○ (D81.3) Adenosine deaminase deficiency (ADA)
○ (D81.4) Nezelof's syndrome
○ (D81.5) Purine nucleoside phosphorylase deficiency (PNP)
○ (D81.6) Major histocompatibility complex class I deficiency
 Bare lymphocyte syndrome
○ (D81.7) Major histocompatibility complex class II deficiency
○ (D81.8) Other combined immunodeficiencies
 Biotin-dependent carboxylase deficiency
○ (D81.9) Combined immunodeficiency, unspecified
 Severe combined immunodeficiency disorder (SCID) NOS
• (D82.) Immunodeficiency associated with other major defects
○ (D82.0) Wiskott-Aldrich syndrome
 Immunodeficiency with thrombocytopenia and eczema
○ (D82.1) Di George's syndrome
○ (D82.2) Immunodeficiency with short-limbed stature
○ (D82.3) Immunodeficiency following hereditary defective response to
Epstein-Barr virus
 X-linked lymphoproliferative disease
○ (D82.4) Hyperimmunoglobulin E syndrome (IgE)
• (D83.) Common variable immunodeficiency
• (D84.) Other immunodeficiencies
○ (D84.0) Lymphocyte function antigen-1 (LFA-1) defect
○ (D84.1) Defects in the complement system
 C1 esterase inhibitor deficiency (C1-INH)
○ (D84.8) Other specified immunodeficiencies
○ (D84.9) Immunodeficiency, unspecified
• (D86.) Sarcoidosis
○ (D86.0) Sarcoidosis of lung
○ (D86.1) Sarcoidosis of lymph nodes
○ (D86.2) Sarcoidosis of lung with sarcoidosis of lymph nodes
○ (D86.3) Sarcoidosis of skin
○ (D86.8) Sarcoidosis of other and combined sites
• (D89.) Other disorders involving the immune mechanism, not elsewhere
classified
○ (D89.0) Polyclonal hypergammaglobulinaemia
 Benign hypergammaglobulinaemic purpura
 Polyclonal gammopathy NOS
○ (D89.1) Cryoglobulinaemia
 ○ (D89.2) Hypergammaglobulinaemia, unspecified
○ (D89.8) Other specified disorders involving the immune mechanism, not
elsewhere classified
○ (D89.9) Disorder involving the immune mechanism, unspecified

[edit] See also

• List of ICD-10 codes
• International Statistical Classification of Diseases and Related Health Problems
• List of ICD-9 codes 140-239: Neoplasms
[edit] References
1. ^ WHO | International Classification of Diseases (ICD)
[show]
v•d•e
Pathology: Medical conditions and ICD code

(Disease / Disorder / Illness, Syndrome / Sequence, Symptom / Sign, Injury, etc.)

(
A
/
B
,

0Infectious disease/Infection: Bacterial disease (G+, G-) · Virus disease · Parasitic disease
0(Protozoan infection, Helminthiasis, Ectoparasitic infestation) · Mycosis · Zoonosis
1
-
1
3
9
)

(Cancer
C(C00-D48, Tumor
/140-239)
D
,Myeloid
hematologic
1(D50-D77, Anemia · Coagulopathy
4280-289)
0
-Lymphoid
2immune
3(D80-D89, Immunodeficiency · Immunoproliferative disorder · Hypersensitivity
9279)

&
2
7
9
-
2
8
9
)

(
E
,

2
4
Endocrine disease · Nutrition disorder · Inborn error of metabolism
0
-
2
7
8
)

(
F
,

2
9
Mental disorder
0
-
3
1
9
)

(
G
,

3
2
Nervous system disease (CNS, PNS) · Neuromuscular disease
0
-
3
5
9
)

(Eye disease · Ear disease

H
,
3
6
0
-
3
8
9
)

(
I
,

3
9
Cardiovascular disease (Heart disease, Vascular disease)
0
-
4
5
9
)

(
J
,

4
6
Respiratory disease (Obstructive lung disease, Restrictive lung disease, Pneumonia)
0
-
5
1
9
)

(
K
,

5
2Stomatognathic disease (Tooth disease) · Digestive disease (Esophageal, Stomach,
0Enteropathy, Liver, Pancreatic)
-
5
7
9
)

(Skin disease · skin appendages (Nail disease, Hair disease, Sweat gland disease)
L
,

6
8
0
-
7
0
9
)

(
M
,

7
1Musculoskeletal disorders: Myopathy · Arthropathy · Osteochondropathy (Osteopathy,
0Chondropathy)
-
7
3
9
)

(
N
,

5
8Urologic disease (Nephropathy, Urinary bladder disease) · Male genital disease · Breast
0disease · Female genital disease
-
6
2
9
)

(
O
,

6
3
Complications of pregnancy · Obstetric labor complication · Puerperal disorder
0
-
6
7
9
)

(Fetal disease
P
,

7
6
0
-
7
7
9
)

(
Q
,

7
4
Congenital disorder (Congenital abnormality)
0
-
7
5
9
)

(
R
,

7
8
Syndromes · Medical signs (Eponymous)
0
-
7
9
9
)

(Bone fracture · Joint dislocation · Sprain · Strain · Subluxation · Head injury · Chest
Strauma · Poisoning
/
T
,

8
0
0
-
9
9
9
)

[show]
v•d•e
Pathology: hematology · hematologic diseases of RBCs and megakaryocytes /
MEP (D50-69,74, 280-287)

↑Polycythemia Polycythemia vera

Micro-: Iron deficiency anemia (Plummer-

Vinson syndrome)
Nutritional
Macro-: Megaloblastic anemia (Pernicious
anemia)

enzymopathy: G6PD · glycolysis

(PK, TI, HK)
hemoglobinopathy: Thalassemia
(alpha, beta, delta) · Sickle-cell
disease/trait · HPFH
R Hereditary membrane:
e Hereditary spherocytosis
d (Minkowski-Chauffard
syndrome) ·
b Hemolytic Hereditary elliptocytosis
l (mostly (Ovalocytosis) · Hereditary
o Normo-) stomatocytosis
oAnemia
d↓
Autoimmune (WAHA, CAD,
c PCH)
e membrane (PNH)
l Acquired MAHA · TM (HUS)
l
s Drug-induced autoimmune · Drug-
induced nonautoimmune
Hemolytic disease of the newborn

Hereditary: Fanconi anemia · Diamond–

Aplastic
Blackfan anemia
(mostly
Normo-) Acquired: PRCA · Sideroblastic anemia ·
Myelophthisic

Blood MCV (Normocytic, Microcytic, Macrocytic) ·

tests MCHC (Normochromic, Hypochromic)

Methemoglobinemia · Sulfhemoglobinemia ·
Other
Reticulocytopenia
CThrombocytosis Essential thrombocytosis
o
a primary: Antithrombin III deficiency · Protein C
g↑ deficiency/Activated protein C resistance/Protein S
uHypercoagulability deficiency/Factor V Leiden · Hyperprothrombinemia
l acquired: DIC (Congenital afibrinogenemia, Purpura fulminans) ·
a autoimmune (Antiphospholipid)
t
i
oThrombocytopenia Nonthrombocytopenic purpura: Henoch-Schönlein purpura
nand purpura Thrombocytopenic purpura: ITP (Evans syndrome) · TM (TTP)
/
Heparin-induced thrombocytopenia · May-Hegglin anomaly
c
↓ adhesion (Bernard-Soulier syndrome) · aggregation (Glanzmann's
o
Platelet function thrombasthenia) · platelet storage pool deficiency (Hermansky-
a
Pudlak syndrome, Gray platelet syndrome)
g
u
l Clotting factor Hemophilia (A/VIII, B/IX, C/XI) • Von Willebrand disease •
o Hypoprothrombinemia/II · XIII
p
a
t
h
y
/

b
l
e
e
d
i
n
g

d
i
a
t
h
e
s
i
s

M: MYL cell/phys (coag, rbmg/mogr/tumr/hist, drug (B1/2/3+5+6),

heme, gran), csfs sysi/epon, btst btst, trns

[show]
v•d•e
 Lymphatic disease: splenic disease (D73/Q89.0, 289.4-289.5/759.0)

A
c
q
u
Acquired asplenia/hyposplenism · Wandering spleen · Splenomegaly (Banti's syndrome)
i
r
e
d

C
o
n
g
e
Congenital asplenia/hyposplenism · Accessory spleen · Polysplenia
n
i
t
a
l

M: LMO anat(h, u, t, a, l)/phys lydi/spdi/thdi/thtu/vatu proc

[show]
v•d•e
Histiocytosis (D76.0, 277.89)

W
Letterer–Siwe disease · Hand–Schüller–Christian disease · Eosinophilic granuloma
H
O
-
I
/
L
a
n
g
e
r
h
a
n
s

c
e
l
l
h
i
s
t
i
o
c
y
t
o
s
i
s

W
H
O
-
I
I
/
n
o
n
-
L
a
n
g
e
r
h
aJuvenile xanthogranuloma · Hemophagocytic lymphohistiocytosis · Erdheim-Chester
ndisease · Niemann-Pick disease · Sea-blue histiocyte syndrome
s

c
e
l
l

h
i
s
t
i
o
c
y
t
o
s
i
s

W
H
O
-
I
I
I
/
m
a
l
i
g
n
a
Histiocytic sarcoma · Langerhans cell sarcoma · Interdigitating dendritic cell sarcoma ·
n
Follicular dendritic cell sarcoma
t

h
i
s
t
i
o
c
y
t
o
s
i
s

U
n
gX-type histiocytosis: Congenital self-healing reticulohistiocytosis
rNon-X histiocytosis: Benign cephalic histiocytosis · Generalized eruptive histiocytoma ·
oXanthoma disseminatum · Progressive nodular histiocytosis · Papular xanthoma ·
uHereditary progressive mucinous histiocytosis · Reticulohistiocytosis (Multicentric
preticulohistiocytosis, Reticulohistiocytoma) · Indeterminate cell histiocytosis
e
d

M: MYL cell/phys (coag, rbmg/mogr/tumr/hist, drug (B1/2/3+5+6),

heme, gran), csfs sysi/epon, btst btst, trns

[show]
v•d•e
Immune disorders: Lymphoid and complement immunodeficiency (D80-D85,
 279.0-4)

X-linked agammaglobulinemia · Transient

Hypogammaglobulinemia
hypogammaglobulinemia of infancy

IgA deficiency · IgG deficiency · IgM

Antibody/humoral deficiency · Hyper IgM syndrome (2, 3, 4,
Dysgammaglobulinemia
(B) 5) · Wiskott-Aldrich syndrome · Hyper-IgE
P syndrome
r
i Common variable immunodeficiency · ICF
Other
m syndrome
a
r thymic hypoplasia: hypoparathyroid (Di George's syndrome) ·
y euparathyroid (Nezelof syndrome, Ataxia telangiectasia)
Cell-mediated (T)
peripheral: Purine nucleoside phosphorylase deficiency · Hyper IgM
syndrome (1)

x-linked: X-SCID
Severe combined
autosomal: Adenosine deaminase deficiency · Omenn syndrome ·
(B+T)
ZAP70 deficiency · Bare lymphocyte syndrome

A
c
q
u
AIDS
i
r
e
d

L
Idiopathic CD4+ lymphocytopenia
e
u
k
o
p
e
n
i
a
:

L
y
m
p
h
o
c
y
t
o
p
e
n
i
a

C
o
m
p
l
e
m
e
n
tC1-inhibitor (Angioedema/Hereditary angioedema) · Complement 2
deficiency/Complement 4 deficiency · Complement 3 deficiency · Terminal complement
dpathway deficiency
e
f
i
c
i
e
n
c
y

M: LMC cell/phys/auag/auab/comp,imrc,tcrp imdf/ipig/hyps/tumr proc, drug(L3/4)

[show]
v•d•e
Sarcoidosis (D86, 135)

I
n
t
e
Annular sarcoidosis · Erythrodermic sarcoidosis · Ichthyosiform sarcoidosis ·
g
Hypopigmented sarcoidosis · Lupus pernio · Morpheaform sarcoidosis · Mucosal
u
sarcoidosis · Papular sarcoid · Scar sarcoid · Subcutaneous sarcoidosis · Ulcerative
e
sarcoidosis
m
e
n
t

C
Neurosarcoidosis
e
n
t
r
a
l

n
e
r
v
o
u
s

s
y
s
t
e
m

L
y
m
p
h
Löfgren syndrome
n
o
d
e

S
y
s
t
Systemic sarcoidosis
e
m
i
c

U
n
g
r
oHeerfordt's syndrome
u
p
e
d
 [show]
v•d•e
Immune disorders, Immunoproliferative immunoglobulin disorders (D89,
273)

P
C
DPlasmacytoma · Multiple myeloma (Plasma cell leukemia) · MGUS · IgM
s(Macroglobulinemia/Waldenström's macroglobulinemia) · heavy chain (Heavy chain
/disease) · light chain (Primary amyloidosis)
P
P

O
t
h
e
r

h
y
p
e
r
g
a
m
Cryoglobulinemia
m
a
g
l
o
b
u
l
i
n
e
m
i
a

M: LMC cell/phys/auag/auab/comp,imrc,tcrp imdf/ipig/hyps/tumr proc, drug(L3/4)

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10_Chapter_III:_Diseases_of_the_blood_and_blood-
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ICD-10 Chapter IV: Endocrine,

nutritional and metabolic diseases
From Wikipedia, the free encyclopedia
Jump to: navigation, search
International Statistical Classification of Diseases and Related Health Problems 10th
Revision
Chapter Blocks Title
I A00-B99 Certain infectious and parasitic diseases
II C00-D48 Neoplasms
D50- Diseases of the blood and blood-forming organs and certain disorders
III
D89 involving the immune mechanism
IV E00-E90 Endocrine, nutritional and metabolic diseases
V F00-F99 Mental and behavioural disorders
G00-
VI Diseases of the nervous system
G99
H00-
VII Diseases of the eye and adnexa
H59
H60-
VIII Diseases of the ear and mastoid process
H95
IX I00-I99 Diseases of the circulatory system
X J00-J99 Diseases of the respiratory system
K00-
XI Diseases of the digestive system
K93
XII L00-L99 Diseases of the skin and subcutaneous tissue
M00-
XIII Diseases of the musculoskeletal system and connective tissue
M99
N00-
XIV Diseases of the genitourinary system
N99
O00-
XV Pregnancy, childbirth and the puerperium
O99
XVI P00-P96 Certain conditions originating in the perinatal period
Q00- Congenital malformations, deformations and chromosomal
XVII
Q99 abnormalities
Symptoms, signs and abnormal clinical and laboratory findings, not
XVIII R00-R99
elsewhere classified
XIX S00-T98 Injury, poisoning and certain other consequences of external causes
V01-
XX External causes of morbidity and mortality
Y98
XXI Z00-Z99 Factors influencing health status and contact with health services
U00-
XXII Codes for special purposes
U99
The International Statistical Classification of Diseases and Related Health Problems 10th
Revision (ICD-10) is a coding of diseases and signs, symptoms, abnormal findings,
complaints, social circumstances and external causes of injury or diseases, as classified
by the World Health Organization (WHO).[1]. This page contains ICD-10 Chapter IV:
Endocrine, nutritional and metabolic diseases.
This is an overview about the chapter IV (also called chapter E) of the International
Statistical Classification of Diseases and Related Health Problems 10th Revision
(ICD-10). This chapter is about Endocrine, nutritional and metabolic diseases.[2]
The ICD-10 is a coding of diseases and signs, symptoms, abnormal findings, complaints,
social circumstances and external causes of injury or diseases, as classified by the World
Health Organization (WHO). The code set allows more than 155,000 different codes and
permits tracking of many new diagnoses and procedures, a significant expansion on the
17,000 codes available in ICD-9.[3]

Contents
[hide]
• 1 E00-E35 - Endocrine diseases
○ 1.1 (E00-E07) Thyroid gland / Thyroid hormone
○ 1.2 (E10-E16) Pancreas / Insulin, glucagon
 1.2.1 (E10-E14) Diabetes mellitus
 1.2.2 (E15-E16) Other disorders of glucose regulation and
pancreatic internal secretion
○ 1.3 (E20-E21) Parathyroid gland / PTH
○ 1.4 (E22-E23) Pituitary gland / ADH, oxytocin, GH, ACTH, TSH, LH,
FSH, prolactin
○ 1.5 (E24-E27) Adrenal gland / Aldosterone, cortisol, epinephrine,
norepinephrine
○ 1.6 (E28-E30) Gonads / Estrogen, androgens, testosterone, etc.
○ 1.7 (E31-E35) Other
• 2 E40-68 - Nutritional diseases
○ 2.1 (E40-E46) Malnutrition
○ 2.2 (E50-E64) Other nutritional deficiencies
○ 2.3 (E65-E68) Obesity and other hyperalimentation
• 3 E70-E90 - Metabolic diseases
○ 3.1 (E70-E79) Metabolic disorders of proteins, fats, and carbohydrates
 3.1.1 (E70-E72) Amino-acids
 3.1.2 (E73-E74) Carbohydrates
 3.1.3 (E75) Lipids
 3.1.4 (E76-E78) Combinations
○ 3.2 (E79-E90) Other metabolic disorders
• 4 See also
• 5 References

[edit] E00-E35 - Endocrine diseases

[edit] (E00-E07) Thyroid gland / Thyroid hormone
• (E00.) Congenital iodine-deficiency syndrome
• (E01.) Iodine-deficiency-related thyroid disorders and allied conditions
○ (E01.0) Iodine-deficiency-related diffuse (endemic) goitre
○ (E01.1) Iodine-deficiency-related multinodular (endemic) goitre
○ (E01.2) Iodine-deficiency-related (endemic) goitre, unspecified
 ○ (E01.8) Other iodine-deficiency-related thyroid disorders and allied
condition
• (E02.) Subclinical iodine-deficiency hypothyroidism
• (E03.) Other hypothyroidism
○ (E03.0) Congenital hypothyroidism with diffuse goitre
○ (E03.1) Congenital hypothyroidism without goitre
○ (E03.2) Hypothyroidism due to medicaments and other exogenous
substances
○ (E03.3) Postinfectious hypothyroidism
○ (E03.4) Atrophy of thyroid (acquired)
○ (E03.5) Myxoedema coma
• (E04.) Other nontoxic goitre
• (E05.) Thyrotoxicosis (hyperthyroidism)
○ (E05.0) Thyrotoxicosis with diffuse goitre
 Graves' disease
○ (E05.1) Thyrotoxicosis with toxic single thyroid nodule
○ (E05.2) Thyrotoxicosis with toxic multinodular goitre
○ (E05.3) Thyrotoxicosis from ectopic thyroid tissue
○ (E05.4) Thyrotoxicosis factitia
○ (E05.5) Thyroid crisis or storm
○ (E05.8) Other thyrotoxicosis
○ (E05.9) Thyrotoxicosis, unspecified
• (E06.) Thyroiditis
○ (E06.0) Acute thyroiditis
○ (E06.1) Subacute thyroiditis
 De Quervain's thyroiditis
○ (E06.2) Chronic thyroiditis with transient thyrotoxicosis
○ (E06.3) Autoimmune thyroiditis
 Hashimoto's thyroiditis
○ (E06.4) Drug-induced thyroiditis
○ (E06.5) Other chronic thyroiditis
 Riedel's thyroiditis
○ (E06.9) Thyroiditis, unspecified
• (E07.) Other disorders of thyroid
○ (E07.0) Hypersecretion of calcitonin
○ (E07.1) Dyshormogenetic goitre
○ (E07.8) Other specified disorders of thyroid
 Sick-euthyroid syndrome
 ○ (E07.9) Disorder of thyroid, unspecified
[edit] (E10-E16) Pancreas / Insulin, glucagon
[edit] (E10-E14) Diabetes mellitus
• Note: the following conditions are subtypes of each code from E10-14:
○ (E1x.0) Diabetic coma
○ (E1x.1) Diabetic ketoacidosis
○ (E1x.2) Diabetic nephropathy
○ (E1x.3) Diabetic retinopathy
○ (E1x.4) Diabetic neuropathy
○ (E1x.5) Diabetic angiopathy
○ (E1x.6) Diabetic arthropathy
• (E10.) Insulin-dependent diabetes mellitus
• (E11.) Non-insulin-dependent diabetes mellitus
• (E12.) Malnutrition-related diabetes mellitus
• (E13.) Other specified diabetes mellitus
• (E14.) Unspecified diabetes mellitus
[edit] (E15-E16) Other disorders of glucose regulation and pancreatic internal
secretion
• (E15.) Nondiabetic hypoglycaemic coma
○
 Drug-induced insulin coma in nondiabetic
 Hyperinsulinism with hypoglycaemic coma
 Hypoglycaemic coma NOS
• (E16.) Other disorders of pancreatic internal secretion
○ (E16.0) Drug-induced hypoglycaemia without coma
○ (E16.1) Other hypoglycaemia
 Functional nonhyperinsulinaemic hypoglycaemia
 Hyperinsulinism: NOS
 Hyperinsulinism: functional
 Hyperplasia of pancreatic islet beta cells NOS
 Posthypoglycaemic coma encephalopathy
○ (E16.2) Hypoglycaemia, unspecified
○ (E16.3) Increased secretion of glucagon
○ (E16.4) Abnormal secretion of gastrin
 Hypergastrinaemia
 Zollinger-Ellison syndrome
○ (E16.8) Other specified disorders of pancreatic internal secretion
 ○ (E16.9) Disorder of pancreatic internal secretion, unspecified
[edit] (E20-E21) Parathyroid gland / PTH
• (E20.) Hypoparathyroidism
○ (E20.0) Idiopathic hypoparathyroidism
○ (E20.1) Pseudohypoparathyroidism
• (E21.) Hyperparathyroidism and other disorders of parathyroid gland
○ (E21.0) Primary hyperparathyroidism
○ (E21.1) Secondary hyperparathyroidism, not elsewhere classified
[edit] (E22-E23) Pituitary gland / ADH, oxytocin, GH, ACTH, TSH, LH,
FSH, prolactin
• (E22.) Hyperfunction of pituitary gland
○ (E22.0) Acromegaly and pituitary gigantism
○ (E22.1) Hyperprolactinaemia
○ (E22.2) Syndrome of inappropriate secretion of antidiuretic hormone
 Central precocious puberty
• (E23.) Hypofunction and other disorders of pituitary gland
○ (E23.0) Hypopituitarism
 Fertile eunuch syndrome
 Hypogonadotropic hypogonadism
 Idiopathic growth hormone deficiency
 Isolated deficiency of gonadotropin
 Isolated deficiency of growth hormone
 Isolated deficiency of pituitary hormone
 Kallmann's syndrome
 Lorain-Levi short stature
 Necrosis of pituitary gland (postpartum)
 Panhypopituitarism
 Pituitary cachexia
 Pituitary insufficiency NOS
 Pituitary short stature
 Sheehan's syndrome
 Simmonds' disease
○ (E23.1) Drug-induced hypopituitarism
○ (E23.2) Diabetes insipidus
○ (E23.3) Hypothalamic dysfunction, not elsewhere classified
○ (E23.6) Other disorders of pituitary gland
 Abscess of pituitary
  Adiposogenital dystrophy
○ (E23.7) Disorder of pituitary gland, unspecified
[edit] (E24-E27) Adrenal gland / Aldosterone, cortisol, epinephrine,
norepinephrine
• (E24.) Cushing's syndrome
○ (E24.0) Pituitary-dependent Cushing's disease
○ (E24.1) Nelson's syndrome
○ (E24.2) Ectopic ACTH syndrome
○ (E24.3) Alcohol-induced pseudo-Cushing's syndrome
○ (E24.4) Other Cushing's syndrome
○ (E24.5) Cushing's syndrome, unspecified
• (E25.) Adrenogenital disorders
○ (E25.0) Congenital adrenogenital disorders associated with enzyme
deficiency
 Congenital adrenal hyperplasia
 Congenital adrenal hyperplasia due to 21-hydroxylase
deficiency
• (E26.) Hyperaldosteronism
○ (E26.0) Primary hyperaldosteronism
 Conn's syndrome
 Primary aldosteronism due to adrenal hyperplasia (bilateral)
○ (E26.1) Secondary hyperaldosteronism
○ (E26.8) Other hyperaldosteronism
 Bartter's syndrome
○ (E26.9) Hyperaldosteronism, unspecified
• (E27.) Other disorders of adrenal gland
○ (E27.0) Other adrenocortical overactivity
○ (E27.1) Primary adrenocortical insufficiency
 Addison's disease
○ (E27.2) Addisonian crisis
○ (E27.3) Drug-induced adrenocortical insufficiency
○ (E27.4) Other and unspecified adrenocortical insufficiency
 Hypoaldosteronism
 Adrenocortical insufficiency NOS
○ (E27.5) Adrenomedullary hyperfunction
[edit] (E28-E30) Gonads / Estrogen, androgens, testosterone, etc.
• (E28.) Ovarian dysfunction
○ (E28.0) Estrogen excess
 ○ (E28.1) Androgen excess
○ (E28.2) Polycystic ovarian syndrome
○ (E28.3) Primary ovarian failure
 Premature menopause NOS
• (E29.) Testicular dysfunction
○ (E29.0) Testicular hyperfunction
○ (E29.1) Testicular hypofunction
 5-Alpha-reductase deficiency (with male pseudohermaphroditism)
 Testicular hypogonadism NOS
• (E30.) Disorders of puberty, not elsewhere classified
○ (E30.0) Delayed puberty
○ (E30.1) Precocious puberty
○ (E30.8) Other disorders of puberty
 Premature thelarche
[edit] (E31-E35) Other
• (E31.) Polyglandular dysfunction
○ (E31.0) Autoimmune polyglandular failure
 Schmidt's syndrome
○ (E31.1) Polyglandular hyperfunction
• (E32.) Diseases of thymus
○ (E32.0) Persistent hyperplasia of thymus
 Hypertrophy of thymus
○ (E32.1) Abscess of thymus
• (E34.) Other endocrine disorders
○ (E34.0) Carcinoid syndrome
○ (E34.1) Other hypersecretion of intestinal hormones
○ (E34.2) Ectopic hormone secretion, not elsewhere classified
○ (E34.3) Short stature, not elsewhere classified
 NOS
 constitutional
 Laron-type
 psychosocial
○ (E34.4) Constitutional tall stature
 Constitutional gigantism
○ (E34.5) Androgen resistance syndrome
 Reifenstein's syndrome
○ (E34.8) Other specified endocrine disorders
  Progeria
• (E35.) Disorders of endocrine glands in diseases classified elsewhere
○ (E35.0) Disorders of thyroid gland in diseases classified elsewhere
○ (E35.1) Disorders of adrenal glands in diseases classified elsewhere
○ (E35.8) Disorders of other endocrine glands in diseases classified
elsewhere
[edit] E40-68 - Nutritional diseases
[edit] (E40-E46) Malnutrition
• (E40.) Kwashiorkor
• (E41.) Nutritional marasmus
• (E42.) Marasmic kwashiorkor
• (E43.) Unspecified severe protein-energy malnutrition
• (E44.) Protein-energy malnutrition of moderate and mild degree
• (E45.) Retarded development following protein-energy malnutrition
• (E46.) Unspecified protein-energy malnutrition
[edit] (E50-E64) Other nutritional deficiencies
• (E50.) Vitamin A deficiency
○ (E50.0) Vitamin A deficiency with conjunctival xerosis
○ (E50.1) Vitamin A deficiency with Bitot's spot and conjunctival xerosis
○ (E50.2) Vitamin A deficiency with corneal xerosis
○ (E50.3) Vitamin A deficiency with corneal ulceration and xerosis
○ (E50.4) Vitamin A deficiency with keratomalacia
○ (E50.5) Vitamin A deficiency with night blindness
○ (E50.6) Vitamin A deficiency with xerophthalmic scars of cornea
○ (E50.7) Other ocular manifestations of vitamin A deficiency
 Xerophthalmia NOS
• (E51.) Thiamine deficiency
○ (E51.1) Beriberi
○ (E51.2) Wernicke's encephalopathy
• (E52.) Niacin deficiency (pellagra)
• (E53.) Deficiency of other B group vitamins
○ (E53.0) Riboflavin deficiency
 Ariboflavinosis
○ (E53.1) Pyridoxine deficiency
○ (E53.8) Deficiency of other specified B group vitamins
• (E54.) Ascorbic acid deficiency
○ Scurvy
 • (E55.) Vitamin D deficiency
○ (E55.0) Rickets, active
• (E56.) Other vitamin deficiencies
○ (E56.0) Deficiency of vitamin E
○ (E56.1) Deficiency of vitamin K
• (E58.) Dietary calcium deficiency
• (E59.) Dietary selenium deficiency
• (E60.) Dietary zinc deficiency
• (E61.) Deficiency of other nutrient elements
○ (E61.1) Iron deficiency
○ (E61.2) Magnesium deficiency
○ (E61.3) Manganese deficiency
○ (E61.4) Chromium deficiency
○ (E61.5) Molybdenum deficiency
○ (E61.6) Vanadium deficiency
• (E63.) Other nutritional deficiencies
○ (E63.0) Essential fatty acid (EFA) deficiency
• (E64.) Sequelae of malnutrition and other nutritional deficiencies
[edit] (E65-E68) Obesity and other hyperalimentation
• (E65.) Localized adiposity
○ Fat pad
• (E66.) Obesity
○ (E66.0) Obesity due to excess calories
○ (E66.1) Drug-induced obesity
○ (E66.2) Extreme obesity with alveolar hypoventilation
 Pickwickian syndrome
○ (E66.8) Other obesity
 Morbid obesity
○ (E66.9) Obesity, unspecified
• (E67.) Other hyperalimentation
○ (E67.0) Hypervitaminosis A
○ (E67.1) Hypercarotenaemia
○ (E67.2) Megavitamin-B 6 syndrome
○ (E67.3) Hypervitaminosis D
• (E68.) Sequelae of hyperalimentation
[edit] E70-E90 - Metabolic diseases
[edit] (E70-E79) Metabolic disorders of proteins, fats, and carbohydrates
[edit] (E70-E72) Amino-acids
• (E70.) Disorders of aromatic amino-acid metabolism
○ (E70.0) Classical phenylketonuria
○ (E70.1) Other hyperphenylalaninaemias
○ (E70.2) Disorders of tyrosine metabolism
 Alkaptonuria (ILDS E70.210)
 Ochronosis (ILDS E70.230)
 Tyrosinaemia
○ (E70.3) Albinism
 Oculocutaneous albinism (ILDS E70.310)
 Partial albinism (ILDS E70.312)
 Oculocutaneous albinism type 1 (tyrosinase-negative) (ILDS
E70.314)
 Oculocutaneous albinism type 2 (tyrosinase positive) (ILDS
E70.314)
 Albinoidism (ILDS E70.318)
 Waardenburg's syndrome (ILDS E70.320)
 Chediak-Higashi syndrome (ILDS E70.340)
 Piebaldism (ILDS E70.350)
 Tietz's syndrome (ILDS E70.358)
 Hermansky-Pudlak syndrome (ILDS E70.360)
 Cross syndrome (ILDS E70.380)
○ (E70.8) Other disorders of aromatic amino-acid metabolism
 Disorders of histidine metabolism
 Disorders of tryptophan metabolism
○ (E70.9) Disorder of aromatic amino-acid metabolism, unspecified
• (E71.) Disorders of branched-chain amino-acid metabolism and fatty-acid
metabolism
○ (E71.0) Maple-syrup-urine disease
○ (E71.1) Other disorders of branched-chain amino-acid metabolism
 Propionic acidemia
 Methylmalonic acidemia
 Isovaleric acidemia
○ (E71.2) Disorder of branched-chain amino-acid metabolism, unspecified
○ (E71.3) Disorders of fatty-acid metabolism
 Adrenoleukodystrophy (Addison-Schilder)
 Muscle carnitine palmityltransferase deficiency
• (E72.) Other disorders of amino-acid metabolism
 ○ (E72.0) Disorders of amino-acid transport
 Cystinuria
 Cystinosis
 Hartnup disease
 Lowe's syndrome
○ (E72.1) Disorders of sulfur-bearing amino-acid metabolism
 Cystathioninuria
 Homocystinuria
 Methioninaemia
 Sulfite oxidase deficiency
○ (E72.2) Disorders of urea cycle metabolism
 Argininaemia
 Argininosuccinic aciduria
 Citrullinaemia
 Hyperammonaemia
○ (E72.3) Disorders of lysine and hydroxylysine metabolism
 Glutaric aciduria
 Hydroxylysinaemia
 Hyperlysinaemia
 Lysinuric protein intolerance
○ (E72.4) Disorders of ornithine metabolism
 Ornithinaemia (types I, II)
○ (E72.5) Disorders of glycine metabolism
 Hyperhydroxyprolinaemia
 Hyperprolinaemia (types I, II)
 Non-ketotic hyperglycinaemia
 Sarcosinaemia
[edit] (E73-E74) Carbohydrates
• (E73.) Lactose intolerance
• (E74.) Other disorders of carbohydrate metabolism
○ (E74.0) Glycogen storage disease
 Glycogen storage disease type I (von Gierke's disease)
 Glycogen storage disease type II (Pompe's disease)
 Glycogen storage disease type III
 Glycogen storage disease type IV
 Glycogen storage disease type V (McArdle's disease)
○ (E74.1) Disorders of fructose metabolism
 Essential fructosuria
  Fructose-1,6-diphosphatase deficiency
 Hereditary fructose intolerance
○ (E74.2) Disorders of galactose metabolism
 Galactosaemia
 Galactokinase deficiency
○ (E74.3) Other disorders of intestinal carbohydrate absorption
 Glucose-galactose malabsorption
 Sucrase deficiency
○ (E74.4) Disorders of pyruvate metabolism and gluconeogenesis
 Deficiency of phosphoenolpyruvate carboxykinase
 Deficiency of pyruvate carboxylase
 Deficiency of pyruvate dehydrogenase
○ (E74.8) Other specified disorders of carbohydrate metabolism
 Essential pentosuria
 Oxalosis
 Oxaluria
 Renal glycosuria
○ (E74.9) Disorder of carbohydrate metabolism, unspecified
[edit] (E75) Lipids
• (E75.) Disorders of sphingolipid metabolism and other lipid storage disorders
○ (E75.0) GM 2 gangliosidosis
 Sandhoff disease
 Tay-Sachs disease
○ (E75.1) Other gangliosidosis
 GM 1
 GM 3
 Mucolipidosis IV
○ (E75.2) Other sphingolipidosis
 Gaucher's disease (ILDS E75.220)
 Niemann-Pick disease (ILDS E75.230)
 Farber's disease (ILDS E75.240)
 Fabry's disease (ILDS E75.250)
○ (E75.3) Sphingolipidosis, unspecified
○ (E75.4) Neuronal ceroid lipofuscinosis
 Batten disease (Type 3)
 Bielschowsky-Jansky disease (Type 2)
 Kufs disease (Type 4)
 Spielmeyer-Vogt disease (Type 3)
 ○ (E75.5) Other lipid storage disorders
 Cerebrotendinous cholesterosis (van Bogaert-Scherer-Epstein)
 Wolman's disease
○ (E75.6) Lipid storage disorder, unspecified
[edit] (E76-E78) Combinations
• (E76.) Disorders of glycosaminoglycan metabolism
○ (E76.0) Mucopolysaccharidosis, type I
 Hurler syndrome
○ (E76.1) Mucopolysaccharidosis, type II
 Hunter syndrome
○ (E76.2) Other mucopolysaccharidoses
 Sanfilippo syndrome
 Morquio syndrome
• (E77.) Disorders of glycoprotein metabolism
○ (E77.0) Defects in post-translational modification of lysosomal enzymes
 Mucolipidosis II (I-cell disease)
 Mucolipidosis III (pseudo-Hurler polydystrophy)
○ (E77.1) Defects in glycoprotein degradation
 Aspartylglucosaminuria
 Fucosidosis
 Mannosidosis
 Sialidosis (mucolipidosis I)
○ (E77.8) Other disorders of glycoprotein metabolism
○ (E77.9) Disorder of glycoprotein metabolism, unspecified
• (E78.) Disorders of lipoprotein metabolism and other lipidaemias
○ (E78.0) Pure hypercholesterolaemia
 Familial hypercholesterolaemia
 Fredrickson's hyperlipoproteinaemia, type IIa
 Hyperbetalipoproteinaemia
 Hyperlipidaemia, group A
 Low-density-lipoprotein-type (LDL) hyperlipoproteinaemia
○ (E78.1) Pure hyperglyceridaemia
 Endogenous hyperglyceridaemia
 Fredrickson's hyperlipoproteinaemia, type IV
 Hyperlipidaemia, group B
 Hyperprebetalipoproteinaemia
 Very-low-density-lipoprotein-type (VLDL) hyperlipoproteinaemia
 ○ (E78.2) Mixed hyperlipidaemia
 Broad- or floating-betalipoproteinaemia
 Fredrickson's hyperlipoproteinaemia, type IIb or III
 Hyperbetalipoproteinaemia with prebetalipoproteinaemia
 Hypercholesterolaemia with endogenous hyperglyceridaemia
 Hyperlipidaemia, group C
 Tubero-eruptive xanthoma
 Xanthoma tuberosum
○ (E78.3) Hyperchylomicronaemia
 Fredrickson's hyperlipoproteinaemia, type I or V
 Hyperlipidaemia, group D
 Mixed hyperglyceridaemia
○ (E78.4) Other hyperlipidaemia
 Familial combined hyperlipidaemia
○ (E78.5) Hyperlipidaemia, unspecified
○ (E78.6) Lipoprotein deficiency
 Abetalipoproteinaemia
 High-density lipoprotein deficiency
 Hypoalphalipoproteinaemia
 Hypobetalipoproteinaemia (familial)
 Lecithin cholesterol acyltransferase deficiency
 Tangier disease
[edit] (E79-E90) Other metabolic disorders
• (E79.) Disorders of purine and pyrimidine metabolism
○ (E79.0) Hyperuricaemia without signs of inflammatory arthritis and
tophaceous disease
○ (E79.1) Lesch-Nyhan syndrome
○ (E79.8) Other disorders of purine and pyrimidine metabolism
 Hereditary xanthinuria
• (E80.) Disorders of porphyrin and bilirubin metabolism
○ (E80.0) Hereditary erythropoietic porphyria
 Erythropoietic protoporphyria (ILDS E80.010)
 Erythropoietic porphyria, congenital (ILDS E80.020)
 Gunther's disease (ILDS (ILDS E80.020)
 Erythropoietic porphyria (ILDS (ILDS E80.030)
 Erythropoietic coproporphyria (ILDS E80.040)
○ (E80.1) Porphyria cutanea tarda
 Sporadic porphyria cutanea tarda (ILDS E80.110)
  Familial porphyria cutanea tarda (ILDS E80.120)
○ (E80.2) Other porphyria
 Acute intermittent porphyria (ILDS E80.210)
 Hereditary coproporphyria (ILDS E80.222)
 Variegate porphyria (ILDS E80.230)
 Chester porphyria (ILDS E80.232)
 Porphyria, hepatic (ILDS E80.240)
 Pseudoporphyria (ILDS E80.250)
 Toxic porphyria (ILDS E80.260)
 Hepatoerythropoietic porphyria (ILDS E80.282)
 Porphyria, NOS (ILDS E80.290)
○ (E80.3) Defects of catalase and peroxidase
 Acatalasia (Takahara)
○ (E80.4) Gilbert's syndrome
○ (E80.5) Crigler-Najjar syndrome
○ (E80.6) Other disorders of bilirubin metabolism
 Dubin-Johnson syndrome
 Rotor's syndrome
○ (E80.7) Disorder of bilirubin metabolism, unspecified
• (E83.) Disorders of mineral metabolism
○ (E83.0) Disorders of copper metabolism
 Wilson's disease
 Menkes disease
○ (E83.1) Disorders of iron metabolism
 Aceruloplasminemia
 Hemochromatosis
○ (E83.2) Disorders of zinc metabolism
 Acrodermatitis enteropathica
○ (E83.3) Disorders of phosphorus metabolism
 Acid phosphatase deficiency
 Familial hypophosphataemia
 Hypophosphatasia
 Vitamin-D-resistant osteomalacia
 Vitamin-D-resistant rickets
○ (E83.4) Disorders of magnesium metabolism
 Hypermagnesemia
 Hypomagnesemia
 ○ (E83.5) Disorders of calcium metabolism
 Familial hypocalciuric hypercalcaemia
 Idiopathic hypercalciuria
• (E84.) Cystic fibrosis
• (E85.) Amyloidosis
○ (E85.0) Non-neuropathic heredofamilial amyloidosis
 Familial Mediterranean fever
 Hereditary amyloid nephropathy
○ (E85.1) Neuropathic heredofamilial amyloidosis
 Amyloid polyneuropathy (Portuguese)
○ (E85.2) Heredofamilial amyloidosis, unspecified
○ (E85.3) Secondary systemic amyloidosis
 Haemodialysis-associated amyloidosis
○ (E85.4) Organ-limited amyloidosis
 Localized amyloidosis
○ (E85.8) Other amyloidosis
○ (E85.9) Amyloidosis, unspecified
• (E86.) Volume depletion
○ Dehydration
○ Hypovolaemia
• (E87.) Other disorders of fluid, electrolyte and acid-base balance
○ (E87.0) Hyperosmolality and hypernatraemia
○ (E87.1) Hypo-osmolality and hyponatraemia
○ (E87.2) Acidosis
 Respiratory acidosis
 Metabolic acidosis
 Lactic acidosis
○ (E87.3) Alkalosis
○ (E87.4) Mixed disorder of acid-base balance
○ (E87.5) Hyperkalaemia
○ (E87.6) Hypokalaemia
○ (E87.7) Fluid overload
○ (E87.8) Other disorders of electrolyte and fluid balance, not elsewhere
classified
 Electrolyte imbalance NOS
 Hyperchloraemia
 Hypochloraemia
 • (E88.) Other metabolic disorders
○ (E88.0) Disorders of plasma-protein metabolism, not elsewhere classified
 Alpha-1-antitrypsin deficiency
 Bisalbuminaemia
○ (E88.1) Lipodystrophy, not elsewhere classified
○ (E88.2) Lipomatosis, not elsewhere classified
○ (E88.8) Other specified metabolic disorders
 Launois-Bensaude adenolipomatosis
 Trimethylaminuria
○ (E88.9) Metabolic disorder, unspecified
• (E89.) Postprocedural endocrine and metabolic disorders, not elsewhere
classified
○ (E89.0) Postprocedural hypothyroidism
○ (E89.1) Postprocedural hypoinsulinaemia
○ (E89.2) Postprocedural hypoparathyroidism
○ (E89.3) Postprocedural hypopituitarism
○ (E89.4) Postprocedural ovarian failure
○ (E89.5) Postprocedural testicular hypofunction
○ (E89.6) Postprocedural adrenocortical(-medullary) hypofunction
• (E90.) Nutritional and metabolic disorders in diseases classified elsewhere
[edit] See also
• List of ICD-10 codes
• International Statistical Classification of Diseases and Related Health Problems
• List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and
immunity disorders
[edit] References
1. ^ WHO | International Classification of Diseases (ICD)
2. ^ http://apps.who.int/classifications/apps/icd/icd10online/?ge65.htm+e66
3. ^ CMS Office of Public Affairs (August 15, 2008). "HHS Proposes Adoption of
ICD-10 Code Sets and Updated Electronic Transaction Standards" (web). News
Release. U.S. Department of Health & Human Services.
http://www.dhhs.gov/news/press/2008pres/08/20080815a.html. Retrieved 2008-
10-22.
v•d•e
Pathology: Medical conditions and ICD code

(Disease / Disorder / Illness, Syndrome / Sequence, Symptom / Sign, Injury, etc.)

(A/B Infectious disease/Infection: Bacterial disease (G+, G-) · Virus disease · Parasitic
, disease (Protozoan infection, Helminthiasis, Ectoparasitic infestation) · Mycosis ·
001-
Zoonosis
139)

Cancer
(C00-D48, Tumor
140-239)
(C/D
, Myeloid
140- hematologic
Anemia · Coagulopathy
239 (D50-D77,
& 280-289)
279-
289) Lymphoid
immune
Immunodeficiency · Immunoproliferative disorder · Hypersensitivity
(D80-D89,
279)

(E,
240- Endocrine disease · Nutrition disorder · Inborn error of metabolism
278)

(F,
290- Mental disorder
319)

(G,
320- Nervous system disease (CNS, PNS) · Neuromuscular disease
359)

(H,
360- Eye disease · Ear disease
389)

(I,
390- Cardiovascular disease (Heart disease, Vascular disease)
459)

(J,
Respiratory disease (Obstructive lung disease, Restrictive lung disease,
460-
Pneumonia)
519)

(K,
Stomatognathic disease (Tooth disease) · Digestive disease (Esophageal, Stomach,
520-
Enteropathy, Liver, Pancreatic)
579)

(L,
680- Skin disease · skin appendages (Nail disease, Hair disease, Sweat gland disease)
709)

(M, Musculoskeletal disorders: Myopathy · Arthropathy · Osteochondropathy

710- (Osteopathy, Chondropathy)
739)

(N,
Urologic disease (Nephropathy, Urinary bladder disease) · Male genital disease ·
580-
Breast disease · Female genital disease
629)

(O,
630- Complications of pregnancy · Obstetric labor complication · Puerperal disorder
679)

(P,
760- Fetal disease
779)

(Q,
740- Congenital disorder (Congenital abnormality)
759)

(R,
780- Syndromes · Medical signs (Eponymous)
799)

(S/T,
Bone fracture · Joint dislocation · Sprain · Strain · Subluxation · Head injury · Chest
800-
trauma · Poisoning
999)

v•d•e
Endocrine pathology: endocrine diseases (E00–35, 240–259)

Diabetes mellitus
types: (type 1, type 2, MODY 1 2 3 4 5 6) · complications
Hypofunction (coma, angiopathy, ketoacidosis, nephropathy, neuropathy,
Pancreas/ retinopathy, cardiomyopathy)
glucose insulin receptor (Rabson–Mendenhall syndrome) · Insulin
metabolism resistance

Hypoglycemia · beta cell (Hyperinsulinism) · G cell

Hyperfunction
(Zollinger–Ellison syndrome)

Hypothalamic/ gonadotropin (Kallmann syndrome, Adiposogenital

pituitary axes dystrophy) · CRH (Tertiary adrenal insufficiency) ·
Hypothalamus
vasopressin (Neurogenic diabetes insipidus) · general
(Hypothalamic hamartoma)

Pituitary anterior (Acromegaly,

Hyperprolactinaemia, Pituitary ACTH
Hyperpituitarism
hypersecretion) · posterior (SIADH) ·
general (Nelson's syndrome)

Hypopituitarism anterior (Kallmann syndrome, Growth

 hormone deficiency, ACTH
deficiency/Secondary adrenal
insufficiency) · posterior (Neurogenic
diabetes insipidus) · general (Empty sella
syndrome, Pituitary apoplexy, Sheehan's
syndrome, Lymphocytic hypophysitis)

Iodine deficiency · Cretinism (Congenital

Hypothyroidism hypothyroidism) · Myxedema · Euthyroid
sick syndrome

Hyperthyroxinemia (Thyroid hormone

resistance, Familial dysalbuminemic
Hyperthyroidism
hyperthyroxinemia) · Hashitoxicosis ·
Thyrotoxicosis factitia · Graves' disease
Thyroid
Acute infectious · Subacute (De
Quervain's, Subacute lymphocytic) ·
Thyroiditis
Autoimmune/chronic (Hashimoto's,
Postpartum, Riedel's)

Endemic goitre · Toxic nodular goitre ·

Goitre Toxic multinodular goitre
Thyroid nodule

Hypoparathyroidism Pseudohypoparathyroidism
Parathyroid
Primary · Secondary · Tertiary ·
Hyperparathyroidism
Osteitis fibrosa cystica

aldosterone: Hyperaldosteronism/Primary
aldosteronism (Conn syndrome, Bartter
syndrome, Glucocorticoid remediable
aldosteronism) · AME · Liddle's syndrome ·
Hyperfunction 17α CAH
cortisol: Cushing's syndrome (Pseudo-
Adrenal Cushing's syndrome)
sex hormones: 21α CAH · 11β CAH

Hypofunction/ aldosterone: Hypoaldosteronism (21α CAH,

Adrenal 11β CAH)
insufficiency
(Addison's, cortisol: CAH (Lipoid, 3β, 11β, 17α, 21α)
WF) sex hormones: 17α CAH

Gonads ovarian: Polycystic ovary syndrome · Premature ovarian

failure
testicular: enzymatic (5-alpha-reductase deficiency, 17-
 beta-hydroxysteroid dehydrogenase deficiency) · Androgen
receptor (Androgen insensitivity syndrome)
general: Hypogonadism (Delayed puberty) ·
Hypergonadism (Precocious puberty)

Height Gigantism · Dwarfism/Short stature (Laron syndrome, Psychosocial)

Autoimmune polyendocrine syndrome (APS1, APS2) · Carcinoid

Multiple syndrome · Multiple endocrine neoplasia (1, 2A, 2B) · Progeria (Werner
syndrome, Acrogeria, Metageria) · Woodhouse-Sakati syndrome

M: END anat/phys/devp/horm/cell noco(d)/cong/tumr, proc, drug

sysi/epon (A10/H1/H2/H3/H5)

v•d•e
Nutrition disorders (E40-68, 260-269)

Protein-
energy Kwashiorkor · Marasmus · Catabolysis
malnutrition

B1: Beriberi/Wernicke's encephalopathy

(Thiamine deficiency) · B2: Ariboflavinosis ·
B B3: Pellagra (Niacin deficiency) ·
vitamins B6: Pyridoxine deficiency · B7: Biotin
deficiency · B9: Folate deficiency · B12: Vitamn
Hypoalimentation/
Avitaminosis B12 deficiency
malnutrition
A: Vitamin A deficiency/Bitot's spots ·
Other C: Scurvy · D: Hypovitaminosis
vitamins D/Rickets/Osteomalacia · E: Vitamin E
deficiency · K: Vitamin K deficiency

Zinc · Iron · Magnesium · Chromium · Selenium

Mineral
(Keshan disease) · Manganese · Molybdenum · Copper ·
deficiency
Calcium · Potassium

Overweight ·Childhood obesity · Obesity hypoventilation syndrome ·

Obesity Abdominal obesity

Vitamin Hypervitaminosis A · Hypervitaminosis D ·

Hyperalimentation
poisoning Hypervitaminosis E

Mineral
see inborn errors of metal metabolism, toxicity
overload

M: NUT cof, enz, met noco, nuvi, sysi/epon, drug(A8/11/12)

met
v•d•e
Inborn error of amino acid metabolism (E70-72, 270)

Lysine/straight Glutaric acidemia type 1 · type 2 · Hyperlysinemia · Pipecolic

chain acidemia · Saccharopinuria

K→acet Maple syrup urine disease · Isovaleric acidemia · 3-

yl-CoA Leucine Methylcrotonyl-CoA carboxylase deficiency · 3-hydroxy-3-
methylglutaryl-CoA lyase deficiency

Tryptophan Hypertryptophanemia

G
Sarcosinemia · D-Glyceric acidemia · Glutathione
G→pyruvate→c synthetase deficiency
Glycine
itrate Glycine→Creatine: GAMT deficiency · Glycine
encephalopathy

Carnosinemia · Histidinemia · Urocanic

Histidine
aciduria
G→glutamate→
α-ketoglutarate Proline Hyperprolinemia · Prolidase deficiency

Glutamate/glutamineSSADHD

Maple syrup urine disease · Hypervalinemia ·

Valine
Isobutyryl-CoA dehydrogenase deficiency

Maple syrup urine disease · Beta-ketothiolase

Isoleucine deficiency · 2-Methylbutyryl-CoA dehydrogenase
G→propionyl-
deficiency
CoA→
succinyl-CoA
Hypermethioninemia · Homocystinuria ·
Methionine
Cystathioninuria

General Propionic acidemia · Methylmalonic acidemia ·

BC/OA Methylmalonyl-CoA mutase deficiency

G→fumarate

Phenylalanine/tyr Tetrahydrobiopterin
osine deficiency · 6-
Phenylketonuria
Pyruvoyltetrahydropte
rin synthase deficiency

Tyrosinemia Type II tyrosinemia ·

Type III
tyrosinemia/Hawkinsi
nuria ·
Alkaptonuria/Ochrono
 sis · Type I
tyrosinemia

Albinism: Ocular
albinism (1) ·
Oculocutaneous
Tyrosine→Melanin albinism (Hermansky–
Pudlak syndrome) ·
Waardenburg
syndrome

Dopamine beta
Tyrosine→Norepine
hydroxylase
phrine
deficiency

N-Acetylglutamate synthase
deficiency · Carbamoyl phosphate
G→oxaloacetate Urea synthetase I deficiency · Ornithine
cycle/Hyperammonemia transcarbamylase
(arginine, aspartate) deficiency/translocase deficiency ·
Citrullinemia · Argininosuccinic
aciduria · Argininemia

Transpo
Solute carrier family: Cystinuria · Hartnup disease · Lysinuric protein
rt/
intolerance · Iminoglycinuria
IE of
RTT Fanconi syndrome: Oculocerebrorenal syndrome · Cystinosis

Other Trimethylaminuria · 2-Hydroxyglutaric aciduria · Fumarase deficiency

M: MET mt, r/g/c/p/i/y, f/s/l/o, rgcp/i/y, f/s/l/o, au, n, m(A16,

a/u, n, h h, epon C10),i(r/g/c/p/i/y, f/s/o,
a/u,n, h)

v•d•e
Inborn error of lipid metabolism: fatty-acid metabolism disorders (E71.3,
277.81-277.85)

Synthesis Biotinidase deficiency

DegradationAcyl
Carnitine (Primary, I, II, -acylcarnitine) · Adrenoleukodystrophy
transport

Beta Acyl CoA dehydrogenase (Short-chain, Medium-

oxidation chain, Long-chain 3-hydroxy, Very long-chain)
General
Mitochondrial trifunctional protein deficiency: Acute
fatty liver of pregnancy
 Unsaturated2,4 Dienoyl-CoA reductase deficiency

Odd chain Propionic acidemia

Other 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

To
acetyl- Malonic aciduria
CoA

AldehydeSjögren-Larsson syndrome

M: MET mt, r/g/c/p/i/y, f/s/l/o, rgcp/i/y, f/s/l/o, au, n, m(A16,

a/u, n, h h, epon C10),i(r/g/c/p/i/y, f/s/o,
a/u,n, h)

v•d•e
Inborn error of carbohydrate metabolism: monosaccharide metabolism
disorders (including glycogen storage diseases) (E73-74, 271)

Disaccharide
Lactose intolerance · Sucrose intolerance
catabolism
Sucrose,
transport
Glucose-galactose malabsorption · Inborn errors of renal
(extracellular)Monosaccharide
tubular transport (Renal glycosuria) · Fructose
transport
malabsorption

fructose: Essential fructosuria · Fructose intolerance

Hexose → Monosaccharide
glucose catabolism galactose/galactosemia : GALK deficiency · GALT
deficiency/GALE deficiency

GSD type 0, glycogen synthase · GSD type IV, Andersen's,

Glycogenesis
branching

Glucose ⇄
extralysosomal: GSD type V, McArdle, muscle glycogen
glycogen
phosphorylase/GSD type VI, Hers', liver glycogen
Glycogenolysis
phosphorylase · GSD type III, Cori's, debranching
lysosomal/LSD: GSD type II, Pompe's, glucosidase

Glucose ⇄ MODY 2 · GSD type VII, Tarui's, phosphofructokinase ·

CAC Glycolysis Triosephosphate isomerase deficiency · Pyruvate kinase
deficiency

Pyruvate
PDHA · Fumarase deficiency
catabolism

GluconeogenesisPCD · Fructose bisphosphatase deficiency · GSD type I,

 von Gierke, glucose 6-phosphatase

Pentose
phosphate Glucose-6-phosphate dehydrogenase deficiency · Pentosuria
pathway

Other Hyperoxaluria (Primary hyperoxaluria)

M: MET mt, r/g/c/p/i/y, f/s/l/o, rgcp/i/y, f/s/l/o, au, n, m(A16,

a/u, n, h h, epon C10),i(r/g/c/p/i/y, f/s/o,
a/u,n, h)

v•d•e
(LSD) Inborn error of lipid metabolism: lipid storage disorders (E75, 272.7-
272.8)

From Ganglioside: GM1 gangliosidoses · GM2

ganglioside gangliosidoses (Sandhoff disease, Tay-Sachs disease,
(gangliosidoses) AB variant)

From globoside Globotriaosylceramide: Fabry's disease

Sphingolipidose From Sphingomyelin: phospholipid: Niemann-Pick disease

s (SMPD1-associated, type C)
sphingomyelin
(to ceramide) Glucocerebroside: Gaucher's disease

From sulfatide Sulfatide: Metachromatic leukodystrophy · Multiple

(sulfatidoses, sulfatase deficiency
leukodystrophy) Galactocerebroside: Krabbe disease

To sphingosine Ceramide: Farber disease

NCL Infantile · Jansky-Bielschowsky disease · Batten disease

Cerebrotendineous xanthomatosis · Cholesteryl ester storage disease

Other
(Wolman disease) · Sea-blue histiocyte syndrome

M: MET mt, r/g/c/p/i/y, f/s/l/o, rgcp/i/y, f/s/l/o, au, n, m(A16,

a/u, n, h h, epon C10),i(r/g/c/p/i/y, f/s/o,
a/u,n, h)

v•d•e
(LSD) Inborn error of carbohydrate metabolism: mucopolysaccharidosis
(E76, 277.5)

Anabolism Pentosuria
Catabolis 1:Hurler/Scheie · 2:Hunter · 3:Sanfilippo ABCD · 4:Morquio · 6:Maroteaux-
m Lamy · 7:Sly

M: MET mt, r/g/c/p/i/y, f/s/l/o, rgcp/i/y, f/s/l/o, au, n, m(A16,

a/u, n, h h, epon C10),i(r/g/c/p/i/y, f/s/o,
a/u,n, h)

v•d•e
(LSD) Inborn error of carbohydrate metabolism: glycoproteinosis (E77,
271.8)

Anabolism Dolichol kinase deficiency · Congenital disorder of glycosylation

Post-
translational
modificatio
n Mucolipidosis: I-cell disease/II · Pseudo-Hurler polydystrophy/III
of
lysosomal
enzymes

Aspartylglucosaminuria · Fucosidosis · mannosidosis (Alpha-mannosidosis,

Catabolism
Beta-mannosidosis) · Sialidosis

Other solute carrier family (Salla disease) · Galactosialidosis

M: MET mt, r/g/c/p/i/y, f/s/l/o, rgcp/i/y, f/s/l/o, au, n, m(A16,

a/u, n, h h, epon C10),i(r/g/c/p/i/y, f/s/o,
a/u,n, h)

v•d•e
Inborn error of lipid metabolism: dyslipidemia (E78, 272.0-272.6)

Hypercholesterolemia/Hypertriglyceridemia (Type I, Familial

Hyperlipidemia hypercholesterolemia/Type IIa, Combined hyperlipidemia/Type
IIb) · Xanthoma/Xanthomatosis

Lecithin cholesterol
Hypoalphalipoproteinemia/HDL acyltransferase deficiency ·
Hypolipoproteinemi Tangier disease
a
Abetalipoproteinemia ·
Hypobetalipoproteinemia/LDL
Apolipoprotein B deficiency

Lipodystrophy Barraquer–Simons syndrome

Other Lipomatosis · Adiposis dolorosa · Lipoid proteinosis

M: MET mt, r/g/c/p/i/y, f/s/l/o, rgcp/i/y, f/s/l/o, au, n, m(A16,

 a/u, n, h h, epon C10),i(r/g/c/p/i/y, f/s/o,
a/u,n, h)

v•d•e
Inborn error of purine-pyrimidine metabolism (E79, 277.2)

Adenylosuccinate lyase deficiency - Myoadenylate deaminase

Anabolism
deficiency
Purine
Nucleotide Lesch-Nyhan syndrome/Hyperuricemia - Adenine
metabolis
salvage phosphoribosyltransferase deficiency
m
Adenosine deaminase deficiency - Purine nucleoside
Catabolism
phosphorylase deficiency - Xanthinuria - Gout

Pyrimidine Anabolism Orotic aciduria

metabolis
m CatabolismDihydropyrimidine dehydrogenase deficiency

M: MET mt, r/g/c/p/i/y, f/s/l/o, rgcp/i/y, f/s/l/o, au, n, m(A16,

a/u, n, h h, epon C10),i(r/g/c/p/i/y, f/s/o,
a/u,n, h)

v•d•e
Heme metabolism disorders (E80, 277.1, 277.4)

early mitochondrial: ALAD porphyria · Acute intermittent porphyria

Porphyria,
hepatic and cytoplasmic: Gunther disease/congenital erythropoietic porphyria ·
erythropoietic Porphyria cutanea tarda/Hepatoerythropoietic porphyria
(porphyrin) late mitochondrial: Hereditary coproporphyria · Variegate porphyria ·
Erythropoietic protoporphyria

Hereditary
unconjugated: Gilbert's syndrome · Crigler-Najjar syndrome · Lucey-
hyperbilirubinemi
Driscoll syndrome
a
(bilirubin) conjugated: Dubin–Johnson syndrome · Rotor syndrome

M: MET mt, r/g/c/p/i/y, f/s/l/o, rgcp/i/y, f/s/l/o, au, n, m(A16,

a/u, n, h h, epon C10),i(r/g/c/p/i/y, f/s/o,
a/u,n, h)

M: MYL cell/phys (coag, rbmg/mogr/tumr/hist, drug (B1/2/3+5+6),

heme, gran), csfs sysi/epon, btst btst, trns

v•d•e
Genetic disorder, organelle: Peroxisomal disorders (E80.3, 277.86)
Peroxisome
Zellweger syndrome · Autosomal adrenoleukodystrophy · Infantile Refsum
biogenesis
disease · Adult Refsum disease-2 · RCP 1
disorder

Enzyme- Acatalasia · RCP 2&3 · Mevalonate kinase deficiency · D-bifunctional

related protein deficiency · Adult Refsum disease-1

Transporter
X-linked adrenoleukodystrophy/Adrenomyeloneuropathy
-related

see also proteins, intermediates

structural (perx, mito, cili, sclr) · DNA/RNA/protein synthesis (drep, trfc) · membrane
(icha, iopu, mtrn) · transduction (csrc, icrc), trfk

v•d•e
Inborn error of metal metabolism (E83, 275)

high: Copper toxicity · Wilson's disease

Cu
deficiency: Copper deficiency · Menkes disease/Occipital horn syndrome

high: Primary iron overload disorder: Hemochromatosis/HFE1 ·

Transition Juvenile/HFE2 · HFE3 · African iron overload/HFE4 ·
Fe
metal Aceruloplasminemia · Atransferrinemia · Hemosiderosis
deficiency: Iron deficiency

high: Zinc toxicity

Zn
deficiency: Acrodermatitis enteropathica

high: Hyperphosphatemia
PO43− deficiency: Hypophosphatemia · alkaline phosphatase
(Hypophosphatasia)

high: Hypermagnesemia
Mg2+
deficiency: Hypomagnesemia
Electrolyt
e
high: Hypercalcaemia · Milk-alkali syndrome (Burnett's) · Calcinosis
(Calciphylaxis, Calcinosis cutis) · Calcification (Metastatic
calcification, Dystrophic calcification) · Familial hypocalciuric
Ca2+ hypercalcemia
deficiency: Hypocalcaemia · Osteomalacia · Pseudohypoparathyroidism
(Albright's hereditary osteodystrophy) ·
Pseudopseudohypoparathyroidism

M: NUT cof, enz, met noco, nuvi, sysi/epon, drug(A8/11/12)

 met

v•d•e
Metabolic disease: amyloidosis (E85, 277.3)

Common
amyloid AA · ATTR · Aβ2M · AL · Aβ/APP · AIAPP · ACal · APro · AANF ·
forming ACys · ABri
proteins

AL amyloidosis · AA amyloidosis · Aβ2M/Haemodialysis-associated

Systemic
amyloidosis · AGel/Finnish type amyloidosis · AA/Familial Mediterranean
amyloidosis
fever · ATTR/Transthyretin-related hereditary amyloidosis

Heart AANF/Isolated atrial amyloidosis

Familial amyloid neuropathy · ACys+ABri/Cerebral amyloid

Brain
angiopathy · Aβ/Alzheimer's disease

Organ- Kidney AApoA1+AFib+ALys/Familial renal amyloidosis

limited
amyloidosisCutaneousPrimary cutaneous amyloidosis · Amyloid purpura

Thyroid: ACal/Medullary thyroid cancer

Endocrine Pituitary: APro/Prolactinoma
Pancreas: AIAPP/Insulinoma · AIAPP/Diabetes mellitus type 2

v•d•e
Water-electrolyte imbalance and acid-base imbalance (E86-E87, 276)

Volume
Volume contraction (Dehydration/Hypovolemia) · Hypervolemia
status

Na+ Hypernatremia · Hyponatremia (Hypotonic, Isotonic)

Electrolyt +
K Hyperkalemia · Hypokalemia
e
Cl− Hyperchloremia · Hypochloremia

Metabolic: High anion gap (Ketoacidosis/Diabetic ketoacidosis,

Acidosis Lactic) · Normal anion gap (Hyperchloremic, Renal tubular)
Respiratory
Acid-base
Metabolic: Contraction alkalosis
Alkalosis
Respiratory

Both Mixed disorder of acid-base balance

 M: URI anat/phys/devp/cell noco/acba/cong/tumr,
sysi/epon, urte

ICD-10 Chapter VI: Diseases of the

nervous system
From Wikipedia, the free encyclopedia
Jump to: navigation, search
International Statistical Classification of Diseases and Related Health Problems 10th
Revision
Chapter Blocks Title
I A00-B99 Certain infectious and parasitic diseases
II C00-D48 Neoplasms
D50- Diseases of the blood and blood-forming organs and certain disorders
III
D89 involving the immune mechanism
IV E00-E90 Endocrine, nutritional and metabolic diseases
V F00-F99 Mental and behavioural disorders
G00-
VI Diseases of the nervous system
G99
H00-
VII Diseases of the eye and adnexa
H59
H60-
VIII Diseases of the ear and mastoid process
H95
IX I00-I99 Diseases of the circulatory system
X J00-J99 Diseases of the respiratory system
K00-
XI Diseases of the digestive system
K93
XII L00-L99 Diseases of the skin and subcutaneous tissue
M00-
XIII Diseases of the musculoskeletal system and connective tissue
M99
N00-
XIV Diseases of the genitourinary system
N99
O00-
XV Pregnancy, childbirth and the puerperium
O99
XVI P00-P96 Certain conditions originating in the perinatal period
Q00- Congenital malformations, deformations and chromosomal
XVII
Q99 abnormalities
Symptoms, signs and abnormal clinical and laboratory findings, not
XVIII R00-R99
elsewhere classified
XIX S00-T98 Injury, poisoning and certain other consequences of external causes
V01-
XX External causes of morbidity and mortality
Y98
XXI Z00-Z99 Factors influencing health status and contact with health services
U00-
XXII Codes for special purposes
U99

The International Statistical Classification of Diseases and Related Health Problems 10th
Revision (ICD-10) is a coding of diseases and signs, symptoms, abnormal findings,
complaints, social circumstances and external causes of injury or diseases, as classified
by the World Health Organization (WHO).[1]. This page contains ICD-10 Chapter VI:
Diseases of the nervous system.

Contents
[hide]
• 1 G00-G99 - Diseases of the nervous system
 ○ 1.1 (G00-G09) Inflammatory diseases of the central nervous system
○ 1.2 (G10-G13) Systemic atrophies primarily affecting the central nervous
system
○ 1.3 (G20-G26) Extrapyramidal and movement disorders
○ 1.4 (G30-G32) Other degenerative diseases of the nervous system
○ 1.5 (G35-G37) Demyelinating diseases of the central nervous system
○ 1.6 (G40-G47) Episodic and paroxysmal disorders
 1.6.1 Epilepsy
 1.6.2 Headaches
 1.6.3 Cerebrovascular
 1.6.4 Sleep disorders
○ 1.7 (G50-G59) Nerve, nerve root and plexus disorders
○ 1.8 (G60-G64) Polyneuropathies and other disorders of the peripheral
nervous system
○ 1.9 (G70-G73) Diseases of myoneural junction and muscle
○ 1.10 (G80-G83) Cerebral palsy and other paralytic syndromes
○ 1.11 (G90-G99) Other disorders of the nervous system
• 2 See also
• 3 References

[edit] G00-G99 - Diseases of the nervous system

[edit] (G00-G09) Inflammatory diseases of the central nervous system
• (G00.) Bacterial meningitis, not elsewhere classified
○ (G00.0) Haemophilus meningitis
○ (G00.1) Pneumococcal meningitis
○ (G00.2) Streptococcal meningitis
○ (G00.3) Staphylococcal meningitis
○ (G00.8) Other bacterial meningitis
 Meningitis due to Escherichia coli
 Meningitis due to Friedländer bacillus
 Meningitis due to Klebsiella
○ (G00.9) Bacterial meningitis, unspecified
• (G01.) Meningitis in bacterial diseases classified elsewhere
• (G02.) Meningitis in other infectious and parasitic diseases classified elsewhere
• (G03.) Meningitis due to other and unspecified causes
○ (G03.0) Nonpyogenic meningitis
○ (G03.1) Chronic meningitis
○ (G03.2) Benign recurrent meningitis (Mollaret)
 ○ (G03.8) Meningitis due to other specified causes
○ (G03.9) Meningitis, unspecified
 Arachnoiditis (spinal) NOS
• (G04.) Encephalitis, myelitis and encephalomyelitis
○ (G04.0) Acute disseminated encephalitis
○ (G04.1) Tropical spastic paraplegia
○ (G04.2) Bacterial meningoencephalitis and meningomyelitis, not
elsewhere classified
○ (G04.8) Other encephalitis, myelitis and encephalomyelitis
○ (G04.9) Encephalitis, myelitis and encephalomyelitis, unspecified
• (G05.) Encephalitis, myelitis and encephalomyelitis in diseases classified
elsewhere
• (G06.) Intracranial and intraspinal abscess and granuloma
• (G07.) Intracranial and intraspinal abscess and granuloma in diseases classified
elsewhere
• (G08.) Intracranial and intraspinal phlebitis and thrombophlebitis
• (G09.) Sequelae of inflammatory diseases of central nervous system
[edit] (G10-G13) Systemic atrophies primarily affecting the central
nervous system
• (G10.) Huntington's disease
• (G11.) Hereditary ataxia
○ (G11.0) Congenital nonprogressive ataxia
○ (G11.1) Early-onset cerebellar ataxia
 Early-onset cerebellar ataxia with essential tremor
 Early-onset cerebellar ataxia with myoclonus (Hunt's ataxia)
 Early-onset cerebellar ataxia with retained tendon reflexes
 Friedreich's ataxia (autosomal recessive)
 X-linked recessive spinocerebellar ataxia
○ (G11.2) Late-onset cerebellar ataxia
○ (G11.3) Cerebellar ataxia with defective DNA repair
 Ataxia telangiectasia (Louis-Bar)
○ (G11.4) Hereditary spastic paraplegia
○ (G11.8) Other hereditary ataxias
○ (G11.9) Hereditary ataxia, unspecified
• (G12.) Spinal muscular atrophy and related syndromes
○ (G12.0) Werdnig-Hoffman disease (Type 1)
○ (G12.1) Other inherited spinal muscular atrophy
 Progressive bulbar palsy of childhood (Fazio-Londe)
  Kugelberg-Welander disease (Type 3)
○ (G12.2) Motor neuron disease
 Familial motor neuron disease
 Amyotrophic lateral sclerosis
 Primary lateral sclerosis
 Progressive bulbar palsy
 Progressive spinal muscular atrophy
• (G13.) Systemic atrophies primarily affecting central nervous system in diseases
classified elsewhere
○ (G13.0) Paraneoplastic neuromyopathy and neuropathy
○ (G13.1) Other systemic atrophy primarily affecting central nervous
system in neoplastic disease
 Paraneoplastic limbic encephalopathy
○ (G13.2) Systemic atrophy primarily affecting central nervous system in
myxoedema
○ (G13.8) Systemic atrophy primarily affecting central nervous system in
other diseases classified elsewhere
[edit] (G20-G26) Extrapyramidal and movement disorders
• (G20.) Parkinson's disease
• (G21.) Secondary parkinsonism
○ (G21.0) Malignant neuroleptic syndrome
○ (G21.3) Postencephalitic parkinsonism
• (G22.) Parkinsonism in diseases classified elsewhere
• (G23.) Other degenerative diseases of basal ganglia
○ (G23.0) Hallervorden-Spatz disease
○ (G23.1) Progressive supranuclear ophthalmoplegia (Steele-Richardson-
Olszewski)
○ (G23.2) Striatonigral degeneration
○ (G23.8) Other specified degenerative diseases of basal ganglia
○ (G23.9) Degenerative disease of basal ganglia, unspecified
• (G24.) Dystonia
○ (G24.0) Drug-induced dystonia
○ (G24.1) Idiopathic familial dystonia
○ (G24.2) Idiopathic nonfamilial dystonia
○ (G24.3) Spasmodic torticollis
○ (G24.4) Idiopathic orofacial dystonia
 Orofacial dyskinesia
○ (G24.5) Blepharospasm
 ○ (G24.8) Other dystonia
○ (G24.9) Dystonia, unspecified
 Dyskinesia NOS
• (G25.) Other extrapyramidal and movement disorders
○ (G25.0) Essential tremor
○ (G25.1) Drug-induced tremor
○ (G25.2) Other specified forms of tremor
○ (G25.3) Myoclonus
○ (G25.4) Drug-induced chorea
○ (G25.5) Other chorea
○ (G25.6) Drug-induced tics and other tics of organic origin
○ (G25.8) Other specified extrapyramidal and movement disorders
 Restless legs syndrome
 Stiff-man syndrome
○ (G25.9) Extrapyramidal and movement disorder, unspecified
• (G26.) Extrapyramidal and movement disorders in diseases classified elsewhere
[edit] (G30-G32) Other degenerative diseases of the nervous system
• (G30.) Alzheimer's disease
• (G31.) Other degenerative diseases of nervous system, not elsewhere classified
○ (G31.0) Circumscribed brain atrophy
 Pick's disease
○ (G31.1) Senile degeneration of brain, not elsewhere classified
○ (G31.2) Degeneration of nervous system due to alcohol
○ (G31.8) Other specified degenerative diseases of nervous system
 Grey-matter degeneration (Alpers)
 Lewy body dementia
 Subacute necrotizing encephalopathy (Leigh)
○ (G31.9) Degenerative disease of nervous system, unspecified
• (G32.) Other degenerative disorders of nervous system in diseases classified
elsewhere
○ (G32.0) Subacute combined degeneration of spinal cord in diseases
classified elsewhere
○ (G32.8) Other specified degenerative disorders of nervous system in
diseases classified elsewhere
[edit] (G35-G37) Demyelinating diseases of the central nervous system
• (G35.) Multiple sclerosis
• (G36.) Other acute disseminated demyelination
○ (G36.0) Neuromyelitis optica (Devic)
 ○ (G36.1) Acute and subacute haemorrhagic leukoencephalitis (Hurst)
○ (G36.8) Other specified acute disseminated demyelination
○ (G36.9) Acute disseminated demyelination, unspecified
• (G37.) Other demyelinating diseases of central nervous system
○ (G37.0) Diffuse sclerosis
○ (G37.1) Central demyelination of corpus callosum
○ (G37.2) Central pontine myelinolysis
○ (G37.3) Acute transverse myelitis in demyelinating disease of central
nervous system
○ (G37.4) Subacute necrotizing myelitis
○ (G37.5) Concentric sclerosis (Baló)
○ (G37.8) Other specified demyelinating diseases of central nervous system
○ (G37.9) Demyelinating disease of central nervous system, unspecified
[edit] (G40-G47) Episodic and paroxysmal disorders
[edit] Epilepsy
• (G40.) Epilepsy
○ (G40.0) Localization-related (focal)(partial) idiopathic epilepsy and
epileptic syndromes with seizures of localized onset
○ (G40.1) Localization-related (focal)(partial) symptomatic epilepsy and
epileptic syndromes with simple partial seizures
○ (G40.2) Localization-related (focal)(partial) symptomatic epilepsy and
epileptic syndromes with complex partial seizures
○ (G40.3) Generalized idiopathic epilepsy and epileptic syndromes
 Benign:
 myoclonic epilepsy in infancy
 neonatal convulsions (familial)
 Childhood absence epilepsy (pyknolepsy)
 Epilepsy with grand mal seizures on awakening
 Juvenile:
 absence epilepsy
 myoclonic epilepsy (impulsive petit mal)
 Nonspecific epileptic seizures:
 atonic
 clonic
 myoclonic
 tonic
 tonic-clonic
○ (G40.4) Other generalized epilepsy and epileptic syndromes
  Epilepsy with:
 myoclonic absences
 myoclonic-astatic seizures
 Infantile spasms
 Lennox-Gastaut syndrome
 Salaam attacks
 Symptomatic early myoclonic encephalopathy
 West's syndrome
○ (G40.5) Special epileptic syndromes
 Epilepsia partialis continua (Kozhevnikov)
○ (G40.6) Grand mal seizures, unspecified (with or without petit mal)
○ (G40.7) Petit mal, unspecified, without grand mal seizures
○ (G40.8) Other epilepsy
 Epilepsies and epileptic syndromes undetermined as to whether
they are focal or generalized
○ (G40.9) Epilepsy, unspecified
• (G41.) Status epilepticus
○ (G41.0) Grand mal status epilepticus
○ (G41.1) Petit mal status epilepticus
○ (G41.2) Complex partial status epilepticus
○ (G41.8) Other status epilepticus
○ (G41.9) Status epilepticus, unspecified
[edit] Headaches
• (G43.) Migraine
○ (G43.0) Migraine without aura (common migraine)
○ (G43.1) Migraine with aura (classical migraine)
○ (G43.2) Status migrainosus
○ (G43.3) Complicated migraine
○ (G43.8) Other migraine
○ (G43.9) Migraine, unspecified
• (G44.) Other headache syndromes
○ (G44.0) Cluster headache syndrome
○ (G44.1) Vascular headache, not elsewhere classified
○ (G44.2) Tension-type headache
○ (G44.3) Chronic post-traumatic headache
○ (G44.4) Drug-induced headache, not elsewhere classified
○ (G44.8) Other specified headache syndromes
[edit] Cerebrovascular
• (G45.) Transient cerebral ischaemic attacks and related syndromes
○ (G45.0) Vertebrobasilar artery syndrome
○ (G45.1) Carotid artery syndrome (hemispheric)
○ (G45.2) Multiple and bilateral precerebral artery syndromes
○ (G45.3) Amaurosis fugax
○ (G45.4) Transient global amnesia
○ (G45.8) Other transient cerebral ischaemic attacks and related syndromes
○ (G45.9) Transient cerebral ischaemic attack, unspecified
• (G46.) Vascular syndromes of brain in cerebrovascular diseases
○ (G46.0) Middle cerebral artery syndrome
○ (G46.1) Anterior cerebral artery syndrome
○ (G46.2) Posterior cerebral artery syndrome
○ (G46.3) Brain stem stroke syndrome
 Benedikt syndrome
 Claude syndrome
 Foville syndrome
 Millard-Gubler syndrome
 Wallenberg syndrome
 Weber syndrome
○ (G46.4) Cerebellar stroke syndrome
○ (G46.5) Pure motor lacunar syndrome
○ (G46.6) Pure sensory lacunar syndrome
○ (G46.7) Other lacunar syndromes
○ (G46.8) Other vascular syndromes of brain in cerebrovascular diseases
[edit] Sleep disorders
• (G47.) Sleep disorders
○ (G47.0) Disorders of initiating and maintaining sleep (insomnias)
○ (G47.1) Disorders of excessive somnolence (hypersomnias)
○ (G47.2) Disruptions in circadian rhythm including jet lag
○ (G47.3) Sleep apnoea
○ (G47.4) Narcolepsy and cataplexy
[edit] (G50-G59) Nerve, nerve root and plexus disorders
• (G50.) Disorders of trigeminal nerve (V)
○ (G50.0) Trigeminal neuralgia
• (G51.) Facial nerve disorders (VII)
○ (G51.0) Bell's palsy
  Facial palsy
○ (G51.1) Geniculate ganglionitis
○ (G51.2) Melkersson's syndrome
 Melkersson-Rosenthal syndrome
○ (G51.3) Clonic hemifacial spasm
○ (G51.4) Facial myokymia
○ (G51.8) Other disorders of facial nerve
○ (G51.8) Disorder of facial nerve, unspecified
• (G52.) Disorders of other cranial nerves
○ (G52.0) Disorders of olfactory nerve (I)
○ (G52.1) Disorders of glossopharyngeal nerve (IX)
○ (G52.2) Disorders of vagus nerve (X)
○ (G52.3) Disorders of hypoglossal nerve (XII)
○ (G52.7) Disorders of multiple cranial nerves
○ (G52.8) Disorders of other specified cranial nerves
○ (G52.9) Cranial nerve disorder, unspecified
• (G53.) Cranial nerve disorders in diseases classified elsewhere
• (G54.) Nerve root and plexus disorders
○ (G54.0) Brachial plexus disorders
 Thoracic outlet syndrome
○ (G54.1) Lumbosacral plexus disorders
○ (G54.2) Cervical root disorders, not elsewhere classified
○ (G54.3) Thoracic root disorders, not elsewhere classified
○ (G54.4) Lumbosacral root disorders, not elsewhere classified
○ (G54.5) Neuralgic Amyotrophy
 Parsonage-Aldren-Turner syndrome
○ (G54.6) Phantom limb syndrome with pain
○ (G54.7) Phantom limb syndrome without pain
• (G55.) Nerve root and plexus compressions in diseases classified elsewhere
• (G56.) Mononeuropathies of upper limb
○ (G56.0) Carpal tunnel syndrome
○ (G56.1) Other lesions of median nerve
○ (G56.2) Lesion of ulnar nerve
 Tardy ulnar nerve palsy
○ (G56.3) Lesion of radial nerve
○ (G56.4) Causalgia
○ (G56.8) Other mononeuropathies of upper limb
  Interdigital neuroma of upper limb
○ (G56.9) Mononeuropathy of upper limb, unspecified
• (G57.) Mononeuropathies of lower limb
○ (G57.0) Lesion of sciatic nerve
○ (G57.1) Meralgia paraesthetica
○ (G57.2) Lesion of femoral nerve
○ (G57.3) Lesion of lateral popliteal nerve
○ (G57.4) Lesion of medial popliteal nerve
○ (G57.5) Tarsal tunnel syndrome
○ (G57.6) Lesion of plantar nerve
 Morton's metatarsalgia
○ (G57.8) Other mononeuropathies of lower limb
○ (G57.9) Mononeuropathy of lower limb, unspecified
• (G58.) Other mononeuropathies
○ (G58.0) Intercostal neuropathy
○ (G58.7) Mononeuritis multiplex
○ (G58.8) Other specified mononeuropathies
○ (G58.9) Mononeuropathy, unspecified
• (G59.) Mononeuropathy in diseases classified elsewhere
[edit] (G60-G64) Polyneuropathies and other disorders of the peripheral
nervous system
• (G60.) Hereditary and idiopathic neuropathy
○ (G60.0) Hereditary motor and sensory neuropathy
 Charcot-Marie-Tooth disease
 Déjerine-Sottas disease
 Hereditary motor and sensory neuropathy, types I-IV
 Hypertrophic neuropathy of infancy
 Peroneal Muscular Atrophy (axonal type)(hypertrophic type)
 Roussy-Lévy syndrome
○ (G60.1) Refsum's disease
○ (G60.2) Neuropathy in association with hereditary ataxia
○ (G60.3) Idiopathic progressive neuropathy
○ (G60.8) Other hereditary and idiopathic neuropathies
 Morvan's disease
 Nelaton's syndrome
 Sensory neuropathy
○ (G60.9) Hereditary and idiopathic neuropathy, unspecified
 • (G61.) Inflammatory polyneuropathy
○ (G61.0) Guillain-Barré syndrome
○ (G61.1) Serum neuropathy
○ (G61.8) Other inflammatory polyneuropathies
○ (G61.9) Inflammatory polyneuropathy, unspecified
• (G62.) Other polyneuropathies
○ (G62.0) Drug-induced polyneuropathy
○ (G62.1) Alcoholic polyneuropathy
○ (G62.2) Polyneuropathy due to other toxic agents
○ (G62.8) Other specified polyneuropathies
○ (G62.9) Polyneuropathy, unspecified
 Neuropathy NOS
• (G63.) Polyneuropathy in diseases classified elsewhere
• (G64.) Other Disorders of peripheral nervous system
[edit] (G70-G73) Diseases of myoneural junction and muscle
• (G70.) Myasthenia gravis and other myoneural disorders
○ (G70.0) Myasthenia gravis
○ (G70.1) Toxic myoneural disorders
○ (G70.2) Congenital and developmental myasthenia
• (G71.) Primary disorders of muscles
○ (G71.0) Muscular dystrophy
 benign muscular dystrophy (Becker muscular dystrophy)
 benign scapuloperoneal muscular dystrophy with early
contractures (Emery-Dreifuss muscular dystrophy)
 distal muscular dystrophy
 facioscapulohumeral muscular dystrophy
 limb-girdle muscular dystrophy
 ocular muscular dystrophy
 oculopharyngeal muscular dystrophy
 scapuloperoneal muscular dystrophy
 severe muscular dystrophy (Duchenne muscular dystrophy)
○ (G71.1) Myotonic disorders
 Dystrophia myotonica (Steinert)
 chondrodystrophic myotonia
 drug-induced myotonia
 symptomatic myotonia
 Myotonia congenita - NOS:
 Myotonia congenita - dominant (Thomsen)
  Myotonia congenita - recessive (Becker)
 Neuromyotonia (Isaacs)
 Paramyotonia congenita
 Pseudomyotonia
○ (G71.2) Congenital myopathies, including:
 Central core disease
 Congenital muscular dystrophy
 Centronuclear myopathy
 Fibre-type disproportion
 Minicore disease
 Multicore disease
 Myotubular myopathy
 Nemaline myopathy
○ (G71.3) Mitochondrial myopathy, not elsewhere classified
• (G72.) Other myopathies
○ (G72.0) Drug-induced myopathy
○ (G72.1) Alcoholic myopathy
○ (G72.2) Myopathy due to other toxic agents
○ (G72.3) Periodic paralysis
 Hypokalemic periodic paralysis
 Hyperkalemic periodic paralysis
• (G73.) Disorders of myoneural junction and muscle in diseases classified
elsewhere
○ (G73.0) Myasthenic syndromes in endocrine diseases
○ (G73.1) Eaton-Lambert syndrome
○ (G73.2) Other myasthenic syndromes in neoplastic disease
○ (G73.3) Myasthenic syndromes in other diseases classified elsewhere
○ (G73.4) Myopathy in infectious and parasitic diseases classified
elsewhere
○ (G73.5) Myopathy in endocrine diseases
○ (G73.6) Myopathy in metabolic diseases
○ (G73.7) Myopathy in other diseases classified elsewhere
[edit] (G80-G83) Cerebral palsy and other paralytic syndromes
• (G80.) Cerebral palsy
○ (G80.0) Spastic quadriplegic cerebral palsy
○ (G80.1) Spastic diplegic cerebral palsy
○ (G80.2) Spastic hemiplegic cerebral palsy
○ (G80.3) Dyskinetic cerebral palsy
 ○ (G80.4) Ataxic cerebral palsy
○ (G80.8) Other cerebral palsy
○ (G80.9) Cerebral palsy, unspecified
• (G81.) Hemiplegia
○ (G81.0) Flaccid hemiplegia
○ (G81.1) Spastic hemiplegia
○ (G81.9) Hemiplegia, unspecified
• (G82.) Paraplegia and tetraplegia
○ (G82.0) Flaccid paraplegia
○ (G82.1) Spastic paraplegia
○ (G82.2) Paraplegia, unspecified
 Paralysis of both lower limbs NOS
 Paraplegia (lower) NOS
○ (G82.3) Flaccid tetraplegia
○ (G82.4) Spastic tetraplegia
○ (G82.5) Tetraplegia, unspecified
 Quadriplegia NOS
• (G83.) Other paralytic syndromes
○ (G83.0) Diplegia of upper limbs
○ (G83.1) Monoplegia of lower limb
○ (G83.2) Monoplegia of upper limb
○ (G83.3) Monoplegia, unspecified
○ (G83.4) Cauda equina syndrome
○ (G83.8) Other specified paralytic syndromes
 Todd's paralysis (postepileptic)
○ (G83.9) Paralytic syndrome, unspecified
[edit] (G90-G99) Other disorders of the nervous system
• (G90.) Disorders of autonomic nervous system
○ (G90.0) Idiopathic peripheral autonomic neuropathy
○ (G90.1) Familial dysautonomia (Riley-Day)
○ (G90.2) Horner's syndrome
○ (G90.3) Multi-system degeneration
○ (G90.8) Other disorders of autonomic nervous system
○ (G90.9) Disorder of autonomic nervous system, unspecified
• (G91.) Hydrocephalus
• (G92.) Toxic encephalopathy
• (G93.) Other disorders of brain
 ○ (G93.0) Cerebral cysts
○ (G93.1) Anoxic brain damage, not elsewhere classified
○ (G93.2) Benign intracranial hypertension
○ (G93.3) Postviral fatigue syndrome
○ (G93.4) Encephalopathy, unspecified
○ (G93.5) Compression of brain
○ (G93.6) Cerebral oedema
○ (G93.7) Reye's syndrome
○ (G93.8) Other specified disorders of brain
 Postradiation encephalopathy
○ (G93.9) Disorder of brain, unspecified
• (G94.) Other disorders of brain in diseases classified elsewhere
• (G95.) Other diseases of spinal cord
○ (G95.0) Syringomyelia and syringobulbia
○ (G95.1) Vascular myelopathies
○ (G95.2) Cord compression, unspecified
○ (G95.8) Other specified diseases of spinal cord
○ (G95.9) Disease of spinal cord, unspecified
 Myelopathy NOS
• (G96.) Other disorders of central nervous system
○ (G96.0) Cerebrospinal fluid leak
○ (G96.1) Disorders of meninges, not elsewhere classified
 Meningeal adhesions (cerebral)(spinal)
○ (G96.8) Other specified disorders of central nervous system
○ (G96.9) Disorder of central nervous system, unspecified
• (G97.) Postprocedural disorders of nervous system, not elsewhere classified
○ (G97.0) Cerebrospinal fluid leak from spinal puncture
○ (G97.1) Other reaction to spinal and lumbar puncture
○ (G97.2) Intracranial hypotension following ventricular shunting
○ (G97.8) Other postprocedural disorders of nervous system
○ (G97.9) Postprocedural disorder of nervous system, unspecified
• (G98.) Other disorders of nervous system, not elsewhere classified
• (G99.) Other disorders of nervous system in diseases classified elsewhere
[edit] See also
• List of ICD-10 codes
• International Statistical Classification of Diseases and Related Health Problems
[edit] References
1. ^ WHO | International Classification of Diseases (ICD)
[show]
v•d•e
Pathology: Medical conditions and ICD code

(Disease / Disorder / Illness, Syndrome / Sequence, Symptom / Sign, Injury, etc.)

(
A
/
B
,

0Infectious disease/Infection: Bacterial disease (G+, G-) · Virus disease · Parasitic disease
0(Protozoan infection, Helminthiasis, Ectoparasitic infestation) · Mycosis · Zoonosis
1
-
1
3
9
)

(Cancer
C(C00-D48, Tumor
/140-239)
D
,Myeloid
hematologic
1(D50-D77, Anemia · Coagulopathy
4280-289)
0
-Lymphoid
2immune
3(D80-D89, Immunodeficiency · Immunoproliferative disorder · Hypersensitivity
9279)

&

2
7
9
-
2
8
9
)

(Endocrine disease · Nutrition disorder · Inborn error of metabolism

E
,

2
4
0
-
2
7
8
)

(
F
,

2
9
Mental disorder
0
-
3
1
9
)

(
G
,

3
2
Nervous system disease (CNS, PNS) · Neuromuscular disease
0
-
3
5
9
)

(
H
,

3
6
Eye disease · Ear disease
0
-
3
8
9
)

(Cardiovascular disease (Heart disease, Vascular disease)

I
,

3
9
0
-
4
5
9
)

(
J
,

4
6
Respiratory disease (Obstructive lung disease, Restrictive lung disease, Pneumonia)
0
-
5
1
9
)

(
K
,

5
2Stomatognathic disease (Tooth disease) · Digestive disease (Esophageal, Stomach,
0Enteropathy, Liver, Pancreatic)
-
5
7
9
)

(
L
,

6
8
Skin disease · skin appendages (Nail disease, Hair disease, Sweat gland disease)
0
-
7
0
9
)
(
M
,

7
1Musculoskeletal disorders: Myopathy · Arthropathy · Osteochondropathy (Osteopathy,
0Chondropathy)
-
7
3
9
)

(
N
,

5
8Urologic disease (Nephropathy, Urinary bladder disease) · Male genital disease · Breast
0disease · Female genital disease
-
6
2
9
)

(
O
,

6
3
Complications of pregnancy · Obstetric labor complication · Puerperal disorder
0
-
6
7
9
)

(
P
,

7
6
Fetal disease
0
-
7
7
9
)
(
Q
,

7
4
Congenital disorder (Congenital abnormality)
0
-
7
5
9
)

(
R
,

7
8
Syndromes · Medical signs (Eponymous)
0
-
7
9
9
)

(
S
/
T
,

8Bone fracture · Joint dislocation · Sprain · Strain · Subluxation · Head injury · Chest
0trauma · Poisoning
0
-
9
9
9
)

[show]
v•d•e
Diseases of meninges (G00–G03, 320–322)

Meningitis/Arachnoiditis: Bacterial (Tuberculous, Haemophilus, Pneumococcal) · Viral

(Herpesviral) · Fungal (Cryptococcal) · Aseptic (Drug-induced)
Meningoencephalitis

M: anat(s,m,p,4,e,b,d,c,a,f,l,g)/p noco(m,d,e,h,v,s)/cong/tumr, proc,drug(N1A/2AB/C/3/4

C hys/devp/cell sysi/epon,injr /7A/B/C/D)
NS

[show]
v•d•e
Pathology of the nervous system, primarily CNS (G04–G47, 323–349)

I Encephalitis (Viral encephalitis, Herpesviral encephalitis) · Cavernous sinus

nBrain thrombosis · Brain abscess (Amoebic)
f
lSpinal Myelitis: Poliomyelitis · Demyelinating disease (Transverse myelitis) ·
acord Tropical spastic paraparesis · Epidural abscess
m
m Encephalomyelitis (Acute disseminated)
aBoth/eitherMeningoencephalitis
t
i
o
n

B
Basal ganglia disease: Parkinsonism (PD,
r
Postencephalitic, NMS) · PKAN · Tauopathy (PSP) ·
a
Striatonigral degeneration · Hemiballismus · HD · OA
i Extrapyramidal
n and Dyskinesia: Dystonia (Status dystonicus, Spasmodic
/ movement torticollis, Meige's, Blepharospasm) · Chorea
disorders (Choreoathetosis) · Myoclonus (Myoclonic epilepsy) ·
e Akathesia
n Tremor (Essential tremor, Intention tremor) · Restless
cDegenerative legs · Stiff person
e
p
h Tauopathy: Alzheimer's (Early-onset) · Frontotemporal
a dementia/Frontotemporal lobar degeneration (Pick's,
Dementia
l Dementia with Lewy bodies)
o Multi-infarct dementia
p
a Mitochondrial
t Leigh's
disease
h
y autoimmune (Multiple sclerosis, Neuromyelitis optica, Schilder's
disease) · hereditary (Adrenoleukodystrophy, Alexander, Canavan,
Demyelinating
Krabbe, ML, PMD, VWM, MFC, CAMFAK syndrome) · Central pontine
myelinolysis · Marchiafava-Bignami disease · Alpers' disease

Episodic/ Focal · Generalised · Status epilepticus · Myoclonic

paroxysmal Seizure/epilepsy
epilepsy

Headache Migraine (Familial hemiplegic) · Cluster · Tension

 TIA (Amaurosis fugax, Transient global amnesia)
Cerebrovascular Stroke (MCA, ACA, PCA, Foville's, Millard-Gubler,
Lateral medullary, Weber's, Lacunar stroke)

Insomnia · Hypersomnia · Sleep apnea (Obstructive,

Ondine's curse) · Narcolepsy · Cataplexy · Kleine-Levin ·
Sleep disorders Circadian rhythm sleep disorder (Advanced sleep phase
syndrome, Delayed sleep phase syndrome, Non-24-hour
sleep-wake syndrome, Jet lag)

Intracranial hypertension (Hydrocephalus/NPH, Idiopathic intracranial

CSF
hypertension) · Cerebral edema · Intracranial hypotension

Brain herniation · Reye's · Hepatic encephalopathy · Toxic

Other
encephalopathy

S
p
i
n
a
l

c
o
r
d
Syringomyelia · Syringobulbia · Morvan's syndrome · Vascular myelopathy (Foix-
/
Alajouanine syndrome) · Spinal cord compression
m
y
e
l
o
p
a
t
h
y

B SA Friedreich's ataxia · Ataxia telangiectasia

o
t
UMN only: PLS · PP · HSP
hDegenerative
/ MNDLMN only: PMA · PBP (Fazio-Londe, Infantile progressive bulbar
e palsy) · SMA (SMN-linked, Kennedy disease, SMAX2, DSMA1)
i both: ALS
t
h
e
r
M: anat(s,m,p,4,e,b,d,c,a,f,l,g)/p noco(m,d,e,h,v,s)/cong/tumr, proc,drug(N1A/2AB/C/3/4
C hys/devp/cell sysi/epon,injr /7A/B/C/D)
NS

[show]
v•d•e
Multiple sclerosis and other demyelinating diseases of CNS (G35–G37, 340–
341)

S
i
g
n
s

a
n
Ataxia · Depression · Diplopia · Dysarthria · Dysphagia · Fatigue · Incontinence ·
d
Neurological fatigue · Nystagmus · Optic neuritis · Pain · Uhthoff's phenomenon ·
Dawson's fingers
s
y
m
p
t
o
m
s

DMcDonald criteria · Poser criteria · EDSS · Clinically isolated syndrome

i
a
g
n
o
s
i
s

a
n
d

e
v
o
l
u
t
i
o
n

f
o
l
l
o
w
i
n
g

I
n
v
e
s
t
iPathophysiology · Experimental autoimmune encephalomyelitis
g
a
t
i
o
n

T
r
e
a
Interferon · Glatiramer acetate · Mitoxantrone · Natalizumab · Therapies under
t
investigation
m
e
n
t

BAcute disseminated encephalomyelitis · Balo concentric sclerosis · Neuromyelitis

ooptica · Guillain-Barré syndrome · Marburg multiple sclerosis · Schilder's disease ·
rTumefactive multiple sclerosis
d
e
r
l
i
n
e

f
o
r
m
s

O
t
hList of people with multiple sclerosis · List of multiple sclerosis organizations
e
r

M: anat(s,m,p,4,e,b,d,c,a,f,l,g)/p noco(m,d,e,h,v,s)/cong/tumr, proc,drug(N1A/2AB/C/3/4

C hys/devp/cell sysi/epon,injr /7A/B/C/D)
NS

[show]
v•d•e
Seizures and epilepsy (G40-G41, 345)

B
a
sSeizure types · Seizure trigger · Breakthrough seizure · Postictal state · Epileptogenesis ·
iAura (warning sign)
c
s

T
r
e
a
tAntiepileptics · Template:Anticonvulsants (for list) · Electroencephalography (diagnosis
mmethod) · Epileptologist
e
n
t
s

R
e
l
a
t
e
d

dTodd's paresis · Landau-Kleffner syndrome · Epilepsy in animals

i
s
o
r
d
e
r
s
E
p
i
l
e
p
s
y

oEpilepsy Foundation (USA) · Epilepsy Toronto · Epilepsy Research UK · Epilepsy

rAction Australia · Citizens United for Research in Epilepsy · Comprehensive Epilepsy
gCenter · David Lewis Centre · Epilepsy Action · National Society for Epilepsy ·
aInternational Dravet Epilepsy Action League
n
i
z
a
t
i
o
n
s

I
s
s
u
e
s

f
o
r
Epilepsy and driving · Epilepsy and employment · Epilepsy in children
e
p
i
l
e
p
t
i
c
s

S Seizures: Simple partial · Complex partial · Jacksonian seizure

ePartial/focal Epilepsy: Temporal lobe epilepsy · Frontal lobe epilepsy · Rolandic
i epilepsy · Nocturnal epilepsy
z
uGeneralised Tonic-clonic · Absence seizure · Atonic seizure · Automatism · Benign
r
e familial neonatal · Lennox-Gastaut · West

tStatus
yepilepticus Epilepsia partialis continua · Complex partial status epilepticus
p
e Progressive myoclonic epilepsy (Dentatorubral-pallidoluysian atrophy,
sMyoclonic Unverricht-Lundborg disease, MERRF syndrome, Lafora disease) ·
epilepsy
Juvenile myoclonic epilepsy
E
pNon-
iepileptic Febrile seizure · Psychogenic non-epileptic seizures
lseizures
e
p
s
y

t
y
p
e
s

M: anat(s,m,p,4,e,b,d,c,a,f,l,g)/p noco(m,d,e,h,v,s)/cong/tumr, proc,drug(N1A/2AB/C/3/4

C hys/devp/cell sysi/epon,injr /7A/B/C/D)
NS

[show]
v•d•e
CNS disease: Headache (G43-G44, 339, 346)

ICHD
Migraine (Familial hemiplegic) · Retinal migraine
1
P
rICHD
Tension
i2
m
aICHD
Cluster · Chronic paroxysmal hemicrania
r3
y
ICHDHemicrania continua · Thunderclap headache · Coital cephalalgia · New daily
4 persistent headache · Hypnic headache

S
e
cICHDIctal headache · Post dural puncture headache
o7
n
dICHDHangover · Medication overuse headache
a8
r
y

I
C
H
Trigeminal neuralgia · Occipital neuralgia · External compression headache · Cold-
D
stimulus headache · Optic neuritis · Postherpetic neuralgia · Tolosa-Hunt syndrome
1
3

O
t
hVascular
e
r

M: anat(s,m,p,4,e,b,d,c,a,f,l,g)/p noco(m,d,e,h,v,s)/cong/tumr, proc,drug(N1A/2AB/C/3/4

C hys/devp/cell sysi/epon,injr /7A/B/C/D)
NS

[show]
v•d•e
CNS disease, Vascular disease: Cerebrovascular diseases (G45-G46 and I60-
I69, 430-438)

B precerebral: Carotid artery stenosis

rTACI,
aPACI cerebral: MCA · ACA · Amaurosis fugax
i Moyamoya disease
n

i precerebral: Anterior spinal artery syndrome · Vertebrobasilar insufficiency

s (Subclavian steal syndrome)
c brainstem: medulla (Medial medullary syndrome, Lateral medullary
hPOCI syndrome) · pons (Medial pontine syndrome/Foville's, Lateral pontine
e syndrome/Millard-Gubler) · midbrain (Weber's, Benedikt, Claude's)
m cerebral: PCA · Lacunar stroke · Thalamic syndrome
i
a cerebellar
/
cerebral: Cerebral venous sinus thrombosis · CADASIL · Binswanger's disease ·
General
c Transient global amnesia
e
r
e
b
r
a
l
i
n
f
a
r
c
t
i
o
n

(
i
s
c
h
e
m
i
c

s
t
r
o
k
e
/
T
I
A
)

IExtra-axial Epidural · Subdural · Subarachnoid

n
tCerebral/Intra-
raxial Intraventricular
a
cBrainstem Duret haemorrhage
r
a
n
i
a
l

h
e
m
o
r
r
h
a
g
e

(
h
e
m
o
r
r
h
a
g
i
c

s
t
r
o
k
e
)

A
n
e
u
Cerebral aneurysm (Intracranial berry aneurysm, Charcot-Bouchard aneurysm)
r
y
s
m

O
t
h
e
r
/
gCerebral vasculitis
e
n
e
r
a
l

M: anat(s,m,p,4,e,b,d,c,a,f,l,g)/p noco(m,d,e,h,v,s)/cong/tumr, proc,drug(N1A/2AB/C/3/4

C hys/devp/cell sysi/epon,injr /7A/B/C/D)
NS

M: anat(a:h,u,t,a,l,v:h,u,t,a,l)/phys/devp/c noco/syva/cong/tu proc,

VA ell/prot mr, sysi/epon drug(C2s/n,C3,C4,C5,C7,C
S 8,C9)

[show]
v•d•e
Psychophysiology: Sleep and sleep disorders (F51 and G47, 307.4 and 327)

S
l
e
e
p
Rapid eye movement sleep · Non-rapid eye movement sleep · Slow-wave sleep
s
t
a
g
e
s

B
r
a
i
n
Alpha wave · Beta wave · Gamma wave · Delta wave · Theta rhythm · K-complex
w
a
v
e
s

S Insomnia · Narcolepsy · Sleep apnea (Obesity hypoventilation

lDyssomnia syndrome, Ondine's curse) · Hypersomnia · Kleine-Levin syndrome ·
e Sleep state misperception
e
pCircadian
Advanced sleep phase syndrome · Delayed sleep phase syndrome ·
rhythm
dsleep disorder Non-24-hour sleep-wake syndrome · Jet lag
i
sParasomnia Night terror · Sleepwalking · Somniloquy
o
rOther/ungroupedNight eating syndrome · Nocturia · Nocturnal myoclonus ·
d
e
r
s
B
e
n
i
g
n
Dream · Exploding head syndrome · False awakening · Hypnagogia · Hypnic jerk ·
p
Lucid dream · Nightmare · Nocturnal emission · Nocturnal penile tumescence · Sleep
h
paralysis · Somnolence
e
n
o
m
e
n
a

R
e
l
aBed (Bunk bed, Four poster bed, Futon, Daybed, Hammock, Mattress, Sleeping bag) ·
tBed bug · Bedding · Bedroom · Bedtime · Bedtime toy · Bedtime story · Caffeine nap ·
eChronotype · Dream journal · Hypnopompic state · Lullaby · Methods of falling asleep ·
dMicrosleep · Nap · Nightwear · Polyphasic sleep · Polysomnography · Power nap ·
Second wind · Siesta · Sleep and creativity · Sleep and learning · Sleep debt · Sleep
tdeprivation · Sleep diary · Sleep inertia · Sleep medicine · Sleeping while on duty ·
oSleepover · Snoring · Excessive daytime sleepiness · ("Sleeping sickness", which is not a sleep
pdisorder.)
i
c
s

M: PSO/PSI mepr dsrd (o, p, m, p, a, proc,

d, s), sysi/epon, drug(N5A/5B/5C/6A/6B/6D)
spvo

M: anat(s,m,p,4,e,b,d,c,a,f,l,g)/p noco(m,d,e,h,v,s)/cong/tumr, proc,drug(N1A/2AB/C/3/4

C hys/devp/cell sysi/epon,injr /7A/B/C/D)
NS

[show]
v•d•e
Nervous system pathology, PNS, Somatic (G50–G64, 350–357)

[hide]

Nerve, nerve root, plexus

Cranial nerve V (Trigeminal neuralgia) · VII (Facial nerve paralysis, Bell's palsy,
 Melkersson–Rosenthal syndrome, Central seven) · XI (Accessory nerve
disease
disorder)

Radiculopathy
brachial plexus (Brachial plexus lesion, Thoracic outlet syndrome) ·
,
Phantom limb
plexopathy

median nerve (Carpal tunnel syndrome, Ape hand deformity)

ulnar nerve (Ulnar nerve entrapment, Froment's sign, Guyon's
Upper canal syndrome, Ulnar claw)
limb radial nerve (Radial neuropathy, Wrist drop, Cheiralgia
paresthetica)
long thoracic nerve (Winged scapula)
Mono-
neuropathy lateral cutaneous nerve of thigh (Meralgia paraesthetica)
tibial nerve (Tarsal tunnel syndrome)
Lower
limb plantar nerve (Morton's neuroma)
superior gluteal nerve (Trendelenburg's sign)
sciatic nerve (Piriformis syndrome)

Causalgia · Mononeuritis multiplex · Neuropathy

General
(Neuralgia/Neuritis) · Nerve compression syndrome

[hide]

Polyneuropathies/Polyradiculoneuropathy

Charcot-Marie-Tooth disease · Dejerine-Sottas disease ·

HMSN
Refsum's disease · Hereditary spastic paraplegia

Autoimmune/demyelinatin Guillain–Barré syndrome · Chronic inflammatory

g demyelinating polyneuropathy

Other Alcoholic polyneuropathy

M: anat(h,r,t,c,b,l,s)/phys/devp/prot/nttr/nttm/ntrp noco/auto/cong/tumr, proc,

PNS sysi/epon, injr drug(N1B)

[show]
v•d•e
Diseases of myoneural junction and muscle / neuromuscular disease (G70-
G73, 358-359)

N autoimmune (Myasthenia gravis, Lambert–Eaton myasthenic syndrome)

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l
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-

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M Limb-girdle muscular dystrophy 1 · Oculopharyngeal ·

y AD
Facioscapulohumeral · Myotonic · Distal (most)
o Muscular
p dystrophy Limb-girdle muscular dystrophy 2 · Congenital (Fukuyama,
a (DAPC) AR
Ullrich, Walker-Warburg)
t
h XRdystrophin (Becker's, Duchenne) · Emerin Emery-Dreifuss
y
/ collagen disease (Bethlem myopathy) · PTP disease (X-linked
Other
MTM) · adaptor protein disease (BIN1-linked centronuclear
c structural myopathy) · cytoskeleton disease (Nemaline myopathy, Zaspopathy)
o
n
Myotonia congenita · Thomsen disease ·
g Myotonia
Neuromyotonia/Isaacs syndrome · Paramyotonia congenita
e
n
ChannelopathyPeriodic
i Hypokalemic (Thyrotoxic) · Hyperkalemic
paralysis
t
a
l Other Central core disease

mMitochondrial MELAS · MERRF · KSS · PEO

y myopathy
o
 p Other Inflammatory myopathy
a
t
h
y

M: MUS, DF+DRCT anat (h/n, u, t/d, a/p, noco(m, s, proc, drug (M1A/3)
l)/phys/hist c)/cong(d)/tumr,
sysi/epon, injr

[show]
v•d•e
Cerebral palsy and other syndromes (G80-G83, 342-344)

P
a
r
e
s
i
s

a
n
dParalysis · Quadriplegia · Triplegia · Hemiplegia/Hemiparesis · Paraplegia/Diplegia ·
Monoplegia
p
l
e
g
i
a

N
O
S

FUpper motor neuron lesion: Pseudobulbar palsy · Spastic diplegia · Spastic paraplegia ·
lHereditary spastic paraplegia
a
cLower motor neuron lesion: Bulbar palsy · Flaccid paralysis
c
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y

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s
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Cerebral palsy · Cauda equina syndrome · Locked-in syndrome
c

t
y
p
e
s

M: anat(s,m,p,4,e,b,d,c,a,f,l,g)/p noco(m,d,e,h,v,s)/cong/tumr, proc,drug(N1A/2AB/C/3/4

C hys/devp/cell sysi/epon,injr /7A/B/C/D)
NS

[show]
v•d•e
Autonomic diseases, Dysautonomia, autonomic- neuropathy (G90, 337)

H
S I · II · III/Familial dysautonomia · IV/Congenital insensitivity to pain with anhidrosis ·
AV
N

O Postural orthostatic tachycardia syndrome · Orthostatic hypotension

r
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a
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 i
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t
Horner's syndrome · Multiple system atrophy · Pure autonomic failure · Autonomic
h
dysreflexia
e
r

M: anat(h,r,t,c,b,l,s)/phys/devp/prot/nttr/nttm/ntrp noco/auto/cong/tumr, proc,

PNS sysi/epon, injr drug(N1B)
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10_Chapter_VI:_Diseases_of_the_nervous_system"
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ICD-10 Chapter V: Mental and

behavioural disorders
From Wikipedia, the free encyclopedia
Jump to: navigation, search
International Statistical Classification of Diseases and Related Health Problems 10th
Revision
Chapter Blocks Title
I A00-B99 Certain infectious and parasitic diseases
II C00-D48 Neoplasms
D50- Diseases of the blood and blood-forming organs and certain disorders
III
D89 involving the immune mechanism
IV E00-E90 Endocrine, nutritional and metabolic diseases
V F00-F99 Mental and behavioural disorders
G00-
VI Diseases of the nervous system
G99
H00-
VII Diseases of the eye and adnexa
H59
H60-
VIII Diseases of the ear and mastoid process
H95
IX I00-I99 Diseases of the circulatory system
X J00-J99 Diseases of the respiratory system
K00-
XI Diseases of the digestive system
K93
XII L00-L99 Diseases of the skin and subcutaneous tissue
M00-
XIII Diseases of the musculoskeletal system and connective tissue
M99
N00-
XIV Diseases of the genitourinary system
N99
O00-
XV Pregnancy, childbirth and the puerperium
O99
XVI P00-P96 Certain conditions originating in the perinatal period
Q00- Congenital malformations, deformations and chromosomal
XVII
Q99 abnormalities
Symptoms, signs and abnormal clinical and laboratory findings, not
XVIII R00-R99
elsewhere classified
XIX S00-T98 Injury, poisoning and certain other consequences of external causes
V01-
XX External causes of morbidity and mortality
Y98
XXI Z00-Z99 Factors influencing health status and contact with health services
U00-
XXII Codes for special purposes
U99

The International Statistical Classification of Diseases and Related Health Problems 10th
Revision (ICD-10) is a coding of diseases and signs, symptoms, abnormal findings,
complaints, social circumstances and external causes of injury or diseases, as classified
by the World Health Organization (WHO).[1]. This page contains ICD-10 Chapter V:
Mental and behavioural disorders.

Contents
[hide]
• 1 F00–F99 – Mental and behavioural disorders
 ○ 1.1 (F00–F09) Organic, including symptomatic, mental disorders
○ 1.2 (F10–F19) Mental and behavioural disorders due to psychoactive
substance use
○ 1.3 (F20–F29) Schizophrenia, schizotypal and delusional disorders
○ 1.4 (F30–F39) Mood (affective) disorders
○ 1.5 (F40–F48) Neurotic, stress-related and somatoform disorders
○ 1.6 (F50–F59) Behavioural syndromes associated with physiological
disturbances and physical factors
○ 1.7 (F60–F69) Disorders of adult personality and behaviour
○ 1.8 (F70–F79) Mental retardation
○ 1.9 (F80–F89) Disorders of psychological development
○ 1.10 (F90–F98) Behavioural and emotional disorders with onset usually
occurring in childhood and adolescence
○ 1.11 (F99) Unspecified mental disorder
• 2 Further reading
• 3 See also
• 4 References

[edit] F00–F99 – Mental and behavioural disorders

[edit] (F00–F09) Organic, including symptomatic, mental disorders
• (F00.) Dementia in Alzheimer's disease
• (F01.) Vascular dementia
○ (F01.1) Multi-infarct dementia
• (F02.) Dementia in other diseases classified elsewhere
○ (F02.0) Dementia in Pick's disease
○ (F02.1) Dementia in Creutzfeldt-Jakob disease
○ (F02.2) Dementia in Huntington's disease
○ (F02.3) Dementia in Parkinson's disease
○ (F02.4) Dementia in human immunodeficiency virus (HIV) disease
• (F03.) Unspecified dementia
• (F04.) Organic amnesic syndrome, not induced by alcohol and other psychoactive
substances
• (F05.) Delirium, not induced by alcohol and other psychoactive substances
• (F06.) Other mental disorders due to brain damage and dysfunction and to
physical disease
○ (F06.0) Organic hallucinosis
○ (F06.1) Organic catatonic disorder
○ (F06.2) Organic delusional (schizophrenia-like) disorder
 ○ (F06.3) Organic mood (affective) disorders
○ (F06.4) Organic anxiety disorder
○ (F06.5) Organic dissociative disorder
○ (F06.6) Organic emotionally labile (asthenic) disorder
○ (F06.7) Mild cognitive disorder
○ (F06.8) Other specified mental disorders due to brain damage and
dysfunction and to physical disease
○ (F06.9) Unspecified mental disorder due to brain damage and dysfunction
and to physical disease
 Organic brain syndrome NOS
• (F07.) Personality and behavioural disorders due to brain disease, damage and
dysfunction
○ (F07.0) Organic personality disorder
○ (F07.1) Postencephalitic syndrome
○ (F07.2) Postconcussional syndrome
○ (F07.8) Other organic personality and behavioural disorders due to brain
disease, damage and dysfunction
○ (F07.9) Unspecified organic personality and behavioural disorder due to
brain disease, damage and dysfunction
• (F09.) Unspecified organic or symptomatic mental disorder
[edit] (F10–F19) Mental and behavioural disorders due to psychoactive
substance use
• Note: the following conditions are subtypes of each code from F10–19:
○ (F1x.0) acute intoxication
○ (F1x.1) harmful use
○ (F1x.2) dependence syndrome
○ (F1x.3) withdrawal state
○ (F1x.4) withdrawal state with delirium
○ (F1x.5) psychotic disorder
○ (F1x.6) amnesic syndrome
○ (F1x.7) Residual and late-onset psychotic disorder
○ (F1x.8) other mental and behavioural disorder
○ (F1x.9) unspecified mental and behavioural disorder
Substan
F1x.0 F1x.1 F1x.2 F1x.3 F1x.4 F1x.5 F1x.6 F1x.7
ce
(F10.) Acute Alcohol Alcohol Alcohol Deliri Alcohol Korsak
use of alcohol abuse dependenc withdrawa um ic off's
alcohol intoxicatio e l treme hallucin syndro
n/ syndrome ns osis me
Alcohol
 intoxicatio
n
(F11.) Opioid
Opioid
use of dependenc
overdose
opioids y
(F12.)
Short-term
use of
effects of
cannabin
cannabis
oids
(F13.)
Benzodiaz
use of Benzodiaz
Benzodiaz Benzodiaz epine
sedatives epine
epine epine drug withdrawa
or dependenc
overdose misuse l
hypnotic e
syndrome
s
(F14.) Cocaine Cocaine
use of intoxicatio dependenc
cocaine n e
(F15.)
use of
Stimula
other
nt
stimulant
psychos
s,
is
including
caffeine
(F16.) Posthalluci
use of nogen
hallucino perception
gens disorder
(F17.) Nicotine
use of withdrawa
tobacco l
(F18.)
use of
volatile
solvents
(F19.)
multiple
drug use
and use
of other
psychoac
tive
substanc
es
[edit] (F20–F29) Schizophrenia, schizotypal and delusional disorders
• (F20.) Schizophrenia
○ (F20.0) Paranoid schizophrenia
○ (F20.1) Hebephrenic schizophrenia (Disorganized schizophrenia)
 ○ (F20.2) Catatonic schizophrenia
○ (F20.3) Undifferentiated schizophrenia
○ (F20.4) Post-schizophrenic depression
○ (F20.5) Residual schizophrenia
○ (F20.6) Simple schizophrenia
○ (F20.8) Other schizophrenia
 Cenesthopathic schizophrenia
 Schizophreniform disorder NOS
 Schizophreniform psychosis NOS
○ (F20.9) Schizophrenia, unspecified
• (F21.) Schizotypal disorder
• (F22.) Persistent delusional disorders
○ (F22.0) Delusional disorder
○ (F22.8) Other persistent delusional disorders
 Delusional dysmorphophobia
 Involutional paranoid state
 Paranoia querulans
○ (F22.9) Persistent delusional disorder, unspecified
• (F23.) Acute and transient psychotic disorders
○ (F23.0) Acute polymorphic psychotic disorder without symptoms of
schizophrenia
○ (F23.1) Acute polymorphic psychotic disorder with symptoms of
schizophrenia
○ (F23.2) Acute schizophrenia-like psychotic disorder
○ (F23.3) Other acute predominantly delusional psychotic disorders
○ (F23.8) Other acute and transient psychotic disorders
○ (F23.9) Acute and transient psychotic disorder, unspecified
• (F24.) Induced delusional disorder
○ Folie à deux
○ Induced paranoid disorder
○ Induced psychotic disorder
• (F25.) Schizoaffective disorders
○ (F25.0) Schizoaffective disorder, manic type
○ (F25.1) Schizoaffective disorder, depressive type
○ (F25.2) Schizoaffective disorder, mixed type
○ (F25.8) Other schizoaffective disorders
○ (F25.9) Schizoaffective disorder, unspecified
• (F28.) Other nonorganic psychotic disorders
 ○ Chronic hallucinatory psychosis
• (F29.) Unspecified nonorganic psychosis
[edit] (F30–F39) Mood (affective) disorders
• (F30.) Manic episode
○ (F30.0) Hypomania
○ (F30.1) Mania without psychotic symptoms
○ (F30.2) Mania with psychotic symptoms
○ (F30.8) Other manic episodes
○ (F30.9) Manic episode, unspecified
• (F31.) Bipolar affective disorder
○ (F31.0) Bipolar affective disorder, current episode hypomanic
○ (F31.1) Bipolar affective disorder, current episode manic without
psychotic symptoms
○ (F31.2) Bipolar affective disorder, current episode manic with psychotic
symptoms
○ (F31.3) Bipolar affective disorder, current episode mild or moderate
depression
○ (F31.4) Bipolar affective disorder, current episode severe depression
without psychotic symptoms
○ (F31.5) Bipolar affective disorder, current episode severe depression with
psychotic symptoms
○ (F31.6) Bipolar affective disorder, current episode mixed
○ (F31.7) Bipolar affective disorder, currently in remission
○ (F31.8) Other bipolar affective disorders
○ (F31.9) Bipolar affective disorder, unspecified
 Bipolar II disorder
 Recurrent manic episodes NOS
○ (F31.9) Bipolar affective disorder, unspecified
• (F32.) Depressive episode
○ (F32.0) Mild depressive episode
○ (F32.1) Moderate depressive episode
○ (F32.2) Severe depressive episode without psychotic symptoms
○ (F32.3) Severe depressive episode with psychotic symptoms
○ (F32.8) Other depressive episodes
 Atypical depression
 Single episodes of "masked" depression NOS
○ (F32.9) Depressive episode, unspecified
• (F33.) Recurrent depressive disorder
 ○ (F33.0) Recurrent depressive disorder, current episode mild
○ (F33.1) Recurrent depressive disorder, current episode moderate
○ (F33.2) Recurrent depressive disorder, current episode severe without
psychotic symptoms
○ (F33.3) Recurrent depressive disorder, current episode severe with
psychotic symptoms
○ (F33.4) Recurrent depressive disorder, currently in remission
○ (F33.8) Other recurrent depressive disorders
○ (F33.9) Recurrent depressive disorder, unspecified
• (F34.) Persistent mood (affective) disorders
○ (F34.0) Cyclothymia
○ (F34.1) Dysthymia
○ (F34.8) Other persistent mood (affective) disorders
○ (F34.9) Persistent mood (affective) disorder, unspecified
• (F38.) Other mood (affective) disorders
○ (F38.0) Other single mood (affective) disorders
 Mixed affective episode
○ (F38.1) Other recurrent mood (affective) disorders
 Recurrent brief depressive episodes
○ (F38.8) Other specified mood (affective) disorders
• (F39.) Unspecified mood (affective) disorder
[edit] (F40–F48) Neurotic, stress-related and somatoform disorders
• (F40.) Phobic anxiety disorders
○ (F40.0) Agoraphobia
○ (F40.1) Social phobias
 Anthropophobia
 Social neurosis
○ (F40.2) Specific (isolated) phobias
 Acrophobia
 Animal phobias
 Claustrophobia
 Simple phobia
○ (F40.8) Other phobic anxiety disorders
○ (F40.9) Phobic anxiety disorder, unspecified
 Phobia NOS
 Phobic state NOS
• (F41.) Other anxiety disorders
○ (F41.0) Panic disorder (episodic paroxysmal anxiety)
 ○ (F41.1) Generalized anxiety disorder
• (F42.) Obsessive-compulsive disorder
• (F43.) Reaction to severe stress, and adjustment disorders
○ (F43.0) Acute stress reaction
○ (F43.1) Post-traumatic stress disorder
○ (F43.2) Adjustment disorder
• (F44.) Dissociative (conversion) disorders
○ (F44.0) Dissociative amnesia
○ (F44.1) Dissociative fugue
○ (F44.2) Dissociative stupor
○ (F44.3) Trance and possession disorders
○ (F44.4) Dissociative motor disorders
○ (F44.5) Dissociative convulsions
○ (F44.6) Dissociative anaesthesia and sensory loss
○ (F44.7) Mixed dissociative (conversion) disorders
○ (F44.8) Other dissociative (conversion) disorders
 Ganser's syndrome
 Multiple personality
○ (F44.9) Dissociative (conversion) disorders, unspecified
• (F45.) Somatoform disorders
○ (F45.0) Somatization disorder
 Briquet's disorder
 Multiple psychosomatic disorder
○ (F45.1) Undifferentiated somatoform disorder
○ (F45.2) Hypochondriacal disorder
 Body dysmorphic disorder
 Dysmorphophobia (nondelusional)
 Hypochondriacal neurosis
 Hypochondriasis
 Nosophobia
○ (F45.3) Somatoform autonomic dysfunction
 Cardiac neurosis
 Da Costa's syndrome
 Gastric neurosis
 Neurocirculatory asthenia
○ (F45.4) Persistent Somatoform Pain Disorder
 Psychalgia
 ○ (F45.8) Other somatoform disorders
○ (F45.9) Somatoform disorder, unspecified
• (F48.) Other neurotic disorders
○ (F48.0) Neurasthenia
○ (F48.1) Depersonalization-derealization syndrome
○ (F48.8) Other specified neurotic disorders
 Dhat syndrome
 Occupational neurosis, including writer's cramp
 Psychasthenia
 Psychasthenic neurosis
 Psychogenic syncope
○ (F48.9) Neurotic disorder, unspecified
 Neurosis NOS
[edit] (F50–F59) Behavioural syndromes associated with physiological
disturbances and physical factors
• (F50.) Eating disorders
○ (F50.0) Anorexia nervosa
○ (F50.1) Atypical anorexia nervosa
○ (F50.2) Bulimia nervosa
○ (F50.3) Atypical bulimia nervosa
○ (F50.4) Overeating associated with other psychological disturbances
○ (F50.5) Vomiting associated with other psychological disturbances
○ (F50.8) Other eating disorders
 Pica in adults
○ (F50.9) Eating disorder, unspecified
• (F51.) Nonorganic sleep disorders
○ (F51.0) Nonorganic insomnia
○ (F51.1) Nonorganic hypersomnia
○ (F51.2) Nonorganic disorder of the sleep-wake schedule
○ (F51.3) Sleepwalking (somnambulism)
○ (F51.4) Sleep terrors (night terrors)
○ (F51.5) Nightmares
• (F52.) Sexual dysfunction, not caused by organic disorder or disease
○ (F52.0) Lack or loss of sexual desire
 Frigidity
 Hypoactive sexual desire disorder
○ (F52.1) Sexual aversion and lack of sexual enjoyment
  Anhedonia (sexual)
○ (F52.2) Failure of genital response
 Female sexual arousal disorder
 Male erectile disorder
 Psychogenic impotence
○ (F52.3) Orgasmic dysfunction
 Inhibited orgasm (male)(female)
 Psychogenic anorgasmy
○ (F52.4) Premature ejaculation
○ (F52.5) Nonorganic vaginismus
○ (F52.6) Nonorganic dyspareunia
○ (F52.7) Excessive sexual drive
○ (F52.8) Other sexual dysfunction, not caused by organic disorder or
disease
○ (F52.9) Unspecified sexual dysfunction, not caused by organic disorder or
disease
• (F53.) Mental and behavioural disorders associated with the puerperium, not
elsewhere classified
○ (F53.0) Mild mental and behavioural disorders associated with the
puerperium, not elsewhere classified
 Postnatal depression NOS
 Postpartum depression NOS
○ (F53.1) Severe mental and behavioural disorders associated with the
puerperium, not elsewhere classified
 Puerperal psychosis NOS
• (F54.) Psychological and behavioural factors associated with disorders or
diseases classified elsewhere
• (F55.) Abuse of non-dependence-producing substances
• (F59.) Unspecified behavioural syndromes associated with physiological
disturbances and physical factors
[edit] (F60–F69) Disorders of adult personality and behaviour
• (F60.) Specific personality disorders
○ (F60.0) Paranoid personality disorder
○ (F60.1) Schizoid personality disorder
○ (F60.2) Dissocial personality disorder
 Antisocial personality disorder
○ (F60.3) Emotionally unstable personality disorder
 Borderline personality disorder
○ (F60.4) Histrionic personality disorder
 ○ (F60.5) Anankastic personality disorder
 Obsessive-compulsive personality disorder
○ (F60.6) Anxious (avoidant) personality disorder
○ (F60.7) Dependent personality disorder
○ (F60.8) Other specific personality disorders
 Eccentric personality disorder
 "Haltlose" type personality disorder
 Immature personality disorder
 Narcissistic personality disorder
 Passive-aggressive personality disorder
 Psychoneurotic personality disorder
○ (F60.9) Personality disorder unspecified
• (F61.) Mixed and other personality disorders
• (F62.) Enduring personality changes, not attributable to brain damage and disease
• (F63.) Habit and impulse disorders
○ (F63.0) Pathological gambling
○ (F63.1) Pathological fire-setting (pyromania)
○ (F63.2) Pathological stealing (kleptomania)
○ (F63.3) Trichotillomania
• (F64.) Gender identity disorders
○ (F64.0) Transsexualism
○ (F64.1) Dual-role transvestism
○ (F64.2) Gender identity disorder of childhood
• (F65.) Disorders of sexual preference
○ (F65.0) Sexual fetishism
○ (F65.1) Fetishistic transvestism
○ (F65.2) Exhibitionism
○ (F65.3) Voyeurism
○ (F65.4) Paedophilia
○ (F65.5) Sadomasochism
○ (F65.6) Multiple disorders of sexual preference
○ (F65.8) Other disorders of sexual preference
 Frotteurism
 Necrophilia
 Zoophilia
• (F66.) Psychological and behavioural disorders associated with sexual
development and orientation
 ○ (F66.0) Sexual maturation disorder
○ (F66.1) Ego-dystonic sexual orientation
○ (F66.2) Sexual relationship disorder
○ (F66.8) Other psychosexual development disorders
○ (F66.9) Psychosexual development disorder, unspecified
• (F68.) Other disorders of adult personality and behaviour
○ (F68.0) Elaboration of physical symptoms for psychological reasons
○ (F68.1) Intentional production or feigning of symptoms or disabilities,
either physical or psychological (factitious disorder)
 Munchausen syndrome
○ (F68.8) Other specified disorders of adult personality and behaviour
• (F69.) Unspecified disorder of adult personality and behaviour
[edit] (F70–F79) Mental retardation
• (F70.) Mild mental retardation
• (F71.) Moderate mental retardation
• (F72.) Severe mental retardation
• (F73.) Profound mental retardation
• (F78.) Other mental retardation
• (F79.) Unspecified mental retardation
[edit] (F80–F89) Disorders of psychological development
• (F80.) Specific developmental disorders of speech and language
○ (F80.0) Specific speech articulation disorder
○ (F80.1) Expressive language disorder
○ (F80.2) Receptive language disorder
 Wernicke's aphasia
○ (F80.3) Acquired aphasia with epilepsy (Landau-Kleffner)
○ (F80.8) Other developmental disorders of speech and language
 Lisping
○ (F80.9) Developmental disorder of speech and language, unspecified
• (F81.) Specific developmental disorders of scholastic skills
○ (F81.0) Specific reading disorder
 Developmental dyslexia
○ (F81.1) Specific spelling disorder
○ (F81.2) Specific disorder of arithmetical skills
 Developmental acalculia
 Gerstmann syndrome
○ (F81.3) Mixed disorder of scholastic skills
 ○ (F81.8) Other developmental disorders of scholastic skills
○ (F81.9) Developmental disorder of scholastic skills, unspecified
• (F82.) Specific developmental disorder of motor function
○ Developmental Dyspraxia
• (F83.) Mixed specific developmental disorders
• (F84.) Pervasive developmental disorders
○ (F84.0) Childhood autism
○ (F84.1) Atypical autism
○ (F84.2) Rett's syndrome
○ (F84.3) Other childhood disintegrative disorder
○ (F84.4) Overactive disorder associated with mental retardation and
stereotyped movements
○ (F84.5) Asperger syndrome
• (F88.) Other disorders of psychological development
• (F89.) Unspecified disorder of psychological development
[edit] (F90–F98) Behavioural and emotional disorders with onset usually
occurring in childhood and adolescence
• (F90.) Hyperkinetic disorders
○ (F90.0) Disturbance of activity and attention
 Attention-deficit hyperactivity disorder
 Attention deficit syndrome with hyperactivity
○ (F90.1) Hyperkinetic conduct disorder
○ (F90.8) Other hyperkinetic disorders
○ (F90.9) Hyperkinetic disorder, unspecified
• (F91.) Conduct disorders
○ (F91.0) Conduct disorder confined to the family context
○ (F91.1) Unsocialized conduct disorder
○ (F91.2) Socialized conduct disorder
○ (F91.3) Oppositional defiant disorder
○ (F91.8) Other conduct disorders
○ (F91.9) Conduct disorder, unspecified
• (F92.) Mixed disorders of conduct and emotions
○ (F92.0) Depressive conduct disorder
○ (F92.8) Other mixed disorders of conduct and emotions
○ (F92.9) Mixed disorder of conduct and emotions, unspecified
• (F93.) Emotional disorders with onset specific to childhood
○ (F93.0) Separation anxiety disorder of childhood
 ○ (F93.1) Phobic anxiety disorder of childhood
○ (F93.2) Social anxiety disorder of childhood
○ (F93.3) Sibling rivalry disorder
○ (F93.8) Other childhood emotional disorders
 Identity disorder
 Overanxious disorder
○ (F93.9) Childhood emotional disorder, unspecified
• (F94.) Disorders of social functioning with onset specific to childhood and
adolescence
○ (F94.0) Elective mutism
○ (F94.1) Reactive attachment disorder of childhood
○ (F94.2) Disinhibited attachment disorder of childhood
○ (F94.8) Other childhood disorders of social functioning
○ (F94.9) Childhood disorder of social functioning, unspecified
• (F95.) Tic disorders
○ (F95.0) Transient tic disorder
○ (F95.1) Chronic motor or vocal tic disorder
○ (F95.2) Combined vocal and multiple motor tic disorder (de la Tourette)
○ (F95.8) Other tic disorders
○ (F95.9) Tic disorder, unspecified
• (F98.) Other behavioural and emotional disorders with onset usually occurring in
childhood and adolescence
○ (F98.0) Nonorganic enuresis
○ (F98.1) Nonorganic encopresis
○ (F98.2) Feeding disorder of infancy and childhood
○ (F98.3) Pica of infancy and childhood
○ (F98.4) Stereotyped movement disorders
○ (F98.5) Stuttering (stammering)
○ (F98.6) Cluttering
○ (F98.8) Other specified behavioural and emotional disorders with onset
usually occurring in childhood and adolescence
 Attention deficit disorder without hyperactivity
 Excessive masturbation
 Nail-biting
 Nose-picking
 Thumb-sucking
○ (F98.9) Unspecified behavioural and emotional disorders with onset
usually occurring in childhood and adolescence
[edit] (F99) Unspecified mental disorder
• (F99.) Mental disorder, not otherwise specified
[edit] Further reading
• Reiersøl O, Skeid S (2006). "The ICD diagnoses of fetishism and
sadomasochism". Journal of homosexuality 50 (2–3): 243–62.
doi:10.1300/J082v50n02_12. PMID 16803767.
[edit] See also
• List of ICD-10 codes
• International Statistical Classification of Diseases and Related Health Problems
• List of ICD-9 codes 290-319: Mental disorders
• Diagnostic classification and rating scales used in psychiatry
[edit] References
1. ^ WHO | International Classification of Diseases (ICD)
[show]
v•d•e
Pathology: Medical conditions and ICD code

(Disease / Disorder / Illness, Syndrome / Sequence, Symptom / Sign, Injury, etc.)

(
A
/
B
,

0Infectious disease/Infection: Bacterial disease (G+, G-) · Virus disease · Parasitic disease
0(Protozoan infection, Helminthiasis, Ectoparasitic infestation) · Mycosis · Zoonosis
1
-
1
3
9
)

(Cancer
C(C00-D48, Tumor
/140-239)
D
,Myeloid
hematologic
1(D50-D77, Anemia · Coagulopathy
4280-289)
0
-Lymphoid Immunodeficiency · Immunoproliferative disorder · Hypersensitivity
2immune
3(D80-D89,
9279)

&

2
7
9
-
2
8
9
)

(
E
,

2
4
Endocrine disease · Nutrition disorder · Inborn error of metabolism
0
-
2
7
8
)

(
F
,

2
9
Mental disorder
0
-
3
1
9
)

(
G
,

3
2
Nervous system disease (CNS, PNS) · Neuromuscular disease
0
-
3
5
9
)
(
H
,

3
6
Eye disease · Ear disease
0
-
3
8
9
)

(
I
,

3
9
Cardiovascular disease (Heart disease, Vascular disease)
0
-
4
5
9
)

(
J
,

4
6
Respiratory disease (Obstructive lung disease, Restrictive lung disease, Pneumonia)
0
-
5
1
9
)

(Stomatognathic disease (Tooth disease) · Digestive disease (Esophageal, Stomach,

KEnteropathy, Liver, Pancreatic)
,

5
2
0
-
5
7
9
)

(
L
,

6
8
Skin disease · skin appendages (Nail disease, Hair disease, Sweat gland disease)
0
-
7
0
9
)

(
M
,

7
1Musculoskeletal disorders: Myopathy · Arthropathy · Osteochondropathy (Osteopathy,
0Chondropathy)
-
7
3
9
)

(
N
,

5
8Urologic disease (Nephropathy, Urinary bladder disease) · Male genital disease · Breast
0disease · Female genital disease
-
6
2
9
)

(Complications of pregnancy · Obstetric labor complication · Puerperal disorder

O
,

6
3
0
-
6
7
9
)

(
P
,

7
6
Fetal disease
0
-
7
7
9
)

(
Q
,

7
4
Congenital disorder (Congenital abnormality)
0
-
7
5
9
)

(
R
,

7
8
Syndromes · Medical signs (Eponymous)
0
-
7
9
9
)

(Bone fracture · Joint dislocation · Sprain · Strain · Subluxation · Head injury · Chest
Strauma · Poisoning
/
T
,

8
0
0
-
9
9
9
)

[show]
v•d•e
Mental and behavioral disorders (F · 290–319)

[show]

Neurological/symptomatic

Mild cognitive impairment · Alzheimer's disease · Multi-infarct dementia ·

Dementi Pick's disease · Creutzfeldt–Jakob disease · Huntington's disease · Parkinson's
a disease · AIDS dementia complex · Frontotemporal dementia · Sundowning,
Wandering

Other Delirium · Post-concussion syndrome · Organic brain syndrome

[show]

Psychoactive substances, substance abuse, drug abuse and substance-related

disorders

Intoxication/Drug overdose · Physical dependence · Substance dependence · Rebound

effect · Double rebound · Withdrawal

[show]

Schizophrenia, schizotypal and delusional

Psychosis (Schizoaffective disorder, Schizophreniform disorder, Brief reactive

psychosis) · Schizophrenia (Disorganized schizophrenia, Delusional disorder, Folie à
deux)

[show]

Mood (affective)

Mania · Bipolar disorder (Bipolar I, Bipolar II, Cyclothymia, Bipolar NOS) · Depression
(Major depressive disorder, Dysthymia, Seasonal affective disorder, Atypical depression,
Melancholic depression)

[show]

Neurotic, stress-related and somatoform

Anxiety Agoraphobia · Social anxiety/Social phobia (Anthropophobia) ·

disorder Phobia
Specific phobia (Claustrophobia) · Specific social phobia
 Panic disorder/Panic attack · Generalized anxiety disorder · OCD ·
Other
stress (Acute stress reaction, PTSD)

Adjustment
Adjustment disorder with depressed mood
disorder

Somatization disorder · Body dysmorphic disorder · Hypochondriasis ·

Somatofor Nosophobia · Da Costa's syndrome · Psychalgia · Conversion disorder
m disorder (Ganser syndrome, Globus pharyngis) · Neurasthenia · Mass Psychogenic
Illness

Dissociative Dissociative identity disorder · Psychogenic amnesia · Fugue state ·

disorder Depersonalization disorder

[show]

Physiological/physical behavioral

Eating
Anorexia nervosa · Bulimia nervosa · Rumination syndrome · NOS
disorder

Nonorgani
c (Nonorganic hypersomnia, Nonorganic insomnia) · Parasomnia (REM
sleep behavior disorder, Night terror, Nightmare)
disorders

Sexual sexual desire (Hypoactive sexual desire disorder, Hypersexuality) · sexual

dysfunctio arousal (Female sexual arousal disorder) · Erectile dysfunction · orgasm
n (Anorgasmia, Premature ejaculation) · pain (Vaginismus, Dyspareunia)

Postnatal Postpartum depression · Postnatal psychosis

[show]

Adult personality and behavior

Sexual
and
Sexual maturation disorder · Ego-dystonic sexual orientation · Sexual relationship
gender
disorder · Paraphilia (Voyeurism, Fetishism)
identit
y

Personality disorder · Impulse control disorder (Kleptomania, Trichotillomania,

Other Pyromania) · Body-focused repetitive behavior · Factitious disorder (Munchausen
syndrome)

[show]

Mental disorders diagnosed in childhood

Mental
Psychological
development
Specific · Pervasive
(developmental
disorder)

ADHD · Conduct disorder (ODD) · emotional disorder (Separation

Emotional and anxiety disorder) · social functioning (Selective mutism, RAD, DAD) ·
behavioral Tic disorder (Tourette syndrome) · Speech (Stuttering, Cluttering) ·
Movement disorder (Stereotypic)

[show]

Symptoms and uncategorized

Catatonia · False pregnancy · Intermittent explosive disorder · Psychomotor agitation ·

Sexual addiction · Stereotypy · Psychogenic non-epileptic seizures · Klüver-Bucy
syndrome

M: PSO/PSI mepr dsrd (o, p, m, p, a, proc,

d, s), sysi/epon, drug(N5A/5B/5C/6A/6B/6D)
spvo

[show]
v•d•e
Psychoactive substance-related disorder (F10–F19, 291–292; 303–305)

G
e
n
SID (Substance intoxication/Drug overdose, Withdrawal, Substance-induced
e
psychosis) · SUD (Substance abuse, Physical dependence/Substance dependence)
r
a
l

A
l
cSID (Alcohol intoxication/Acute, Alcohol withdrawal, Delirium tremens, Alcoholic
ohallucinosis, Korsakoff's syndrome) · Alcoholism/SUD (Alcohol abuse, Alcohol
hdependence)
o
l

O
p
i
oSID (Opioid overdose) · SUD (Opioid dependence)
i
d
s
C
a
n
nSID (Short-term effects of cannabis/toxicity, Cannabis withdrawal) · SUD (Cannabis
adependence)
b
i
s

S
e
d
a
t
i
v
ebenzodiazepine: SID (Benzodiazepine overdose, Benzodiazepine withdrawal) · SUD
/(Benzodiazepine drug misuse, Benzodiazepine dependence)
hbarbiturate: SID (Barbiturate overdose) · SUD (Barbiturate dependence)
y
p
n
o
t
i
c

C
o
c
aSID (Cocaine intoxication) · SUD (Cocaine dependence)
i
n
e

S
t
i
m
u
SID (Stimulant psychosis) · SUD (Amphetamine dependence)
l
a
n
t
s

H
SID (Hallucinogen persisting perception disorder)
a
l
l
u
c
i
n
o
g
e
n

T
o
b
aSID (Nicotine poisoning, Nicotine withdrawal)
c
c
o

V
o
l
a
t
i
l
e
Inhalant abuse: Toluene toxicity
s
o
l
v
e
n
t
s

M
u
l
t
Poly drug use
i
p
l
e

M: PSO/PSI mepr dsrd (o, p, m, p, a, proc,

d, s), sysi/epon, drug(N5A/5B/5C/6A/6B/6D)
spvo

[show]
v•d•e
Mood disorder (F30–F39, 296)
H
i
s
Emil Kraepelin · Karl Leonhard · John Cade · Mogens Schou · Frederick K. Goodwin ·
t
Kay Redfield Jamison
o
r
y

S
y
m
pHallucination · Delusion · Emotional dysregulation (Anhedonia, Dysphoria, Suicidal
tideation) · sleep disorder (Hypersomnia, Insomnia) · Psychosis · Racing thoughts
o
m
s

S
p
e
Bipolar disorder (Bipolar I, Bipolar II, Bipolar NOS) · Cyclothymia · Dysthymia · Major
c
depressive disorder · Schizoaffective disorder
t
rMania · Mixed state · Hypomania · Major depressive episode · Rapid cycling
u
m

Carbamazepine · Gabapentin · Lamotrigine · Oxcarbazepine ·

TAnticonvulsants
Topiramate · Valproic acid (Sodium valproate, Valproate semisodium)
r
eOther mood Lithium pharmacology (Lithium carbonate, Lithium citrate, Lithium
astabilizers sulfate) · Antipsychotics
t
m
e Clinical psychology · Electroconvulsive therapy · Involuntary
nNon- commitment · Light therapy · Psychotherapy · Transcranial magnetic
tpharmaceutical stimulation
· Cognitive behavioral therapy

R
e
l
Affective spectrum · List of people affected by bipolar disorder · Bipolar disorder in
a
children · Book:Bipolar Disorder
t
e
d

M: PSO/PSI mepr dsrd (o, p, m, p, a, proc,

d, s), sysi/epon, drug(N5A/5B/5C/6A/6B/6D)
spvo
 [show]
v•d•e
Anxiety disorder: Obsessive–compulsive disorder (F42, 300.3)
H
i
s
tYale–Brown Obsessive Compulsive Scale
o
r
y

B Basal ganglia (striatum) · Orbitofrontal cortex · Cingulate cortex · Brain-

iNeuroanatomy derived neurotrophic factor
o
l 5-HT1Dβ · 5-HT2A · 5-HT2C · μ Opioid · H2 · NK1 · M4 · NMDA · non-
oReceptors NMDA
g
y

S
y
m
Obsessions (associative, diagnostic, injurious, scrupulous, pathogenic, sexual) ·
p
Compulsions (impulses, rituals, tics) · Thought suppression (avoidance) · Hoarding
t
(animals, books, possessions)
o
m
s

T Selective
r serotonin Escitalopram · Fluoxetine · Fluvoxamin · Paroxetine ·
e reuptake Sertraline · Citalopram · Nefazodone
a inhibitors
t
m Serotonin-
e norepinephrine
n Venlafaxine · Desvenlafaxine · Duloxetine
reuptake
t inhibitors

Serotonergics Monoamine
oxidase Phenelzine · Tranylcypromine
inhibitors

Tricyclic
Clomipramine
antidepressants

Serotonergic
Lysergic acid diethylamide · Psilocin
psychedelics

Nootropics Inositol

Mu opioidergics Hydrocodone · Morphine · Tramadol

AnticholinergicsDiphenhydramine
NMDA
Riluzole
glutamatergics

NK-1
Aprepitant
tachykininergics

Other Nicotine · Memantine · Tautomycin

Behavioral Cognitive behavioral therapy (Exposure and response prevention)

O
r
g
a
n
i
zOCD Action
a
t
i
o
n
s

N
o
t
a
b
l
eEdna B. Foa · Stanley Rachman · Adam S. Radomsky · Jeffrey M. Schwartz · Susan
Swedo
p
e
o
p
l
e

P Fictional Matchstick Men · Plyushkin

oLiterature
p NonfictionEverything in Its Place
u
lMedia Monk · As Good as It Gets · Matchstick Men · The Aviator · Adrian Monk
a
r

c
u
l
t
u
r
e

R
e
l
Obsessive–compulsive personality disorder · Obsessional jealousy · Purely Obsessional
a
OCD · Social anxiety disorder · Tourette syndrome
t
e
d

M: PSO/PSI mepr dsrd (o, p, m, p, a, proc,

d, s), sysi/epon, drug(N5A/5B/5C/6A/6B/6D)
spvo

[show]
v•d•e
Psychophysiology: Sleep and sleep disorders (F51 and G47, 307.4 and 327)

S
l
e
e
p
Rapid eye movement sleep · Non-rapid eye movement sleep · Slow-wave sleep
s
t
a
g
e
s

B
r
a
i
n
Alpha wave · Beta wave · Gamma wave · Delta wave · Theta rhythm · K-complex
w
a
v
e
s

S Insomnia · Narcolepsy · Sleep apnea (Obesity hypoventilation

lDyssomnia syndrome, Ondine's curse) · Hypersomnia · Kleine-Levin syndrome ·
e Sleep state misperception
e
pCircadian Advanced sleep phase syndrome · Delayed sleep phase syndrome ·
 rhythm
dsleep disorder Non-24-hour sleep-wake syndrome · Jet lag
i
sParasomnia Night terror · Sleepwalking · Somniloquy
o
rOther/ungroupedNight eating syndrome · Nocturia · Nocturnal myoclonus ·
d
e
r
s

B
e
n
i
g
n
Dream · Exploding head syndrome · False awakening · Hypnagogia · Hypnic jerk ·
p
Lucid dream · Nightmare · Nocturnal emission · Nocturnal penile tumescence · Sleep
h
paralysis · Somnolence
e
n
o
m
e
n
a

R
e
l
aBed (Bunk bed, Four poster bed, Futon, Daybed, Hammock, Mattress, Sleeping bag) ·
tBed bug · Bedding · Bedroom · Bedtime · Bedtime toy · Bedtime story · Caffeine nap ·
eChronotype · Dream journal · Hypnopompic state · Lullaby · Methods of falling asleep ·
dMicrosleep · Nap · Nightwear · Polyphasic sleep · Polysomnography · Power nap ·
Second wind · Siesta · Sleep and creativity · Sleep and learning · Sleep debt · Sleep
tdeprivation · Sleep diary · Sleep inertia · Sleep medicine · Sleeping while on duty ·
oSleepover · Snoring · Excessive daytime sleepiness · ("Sleeping sickness", which is not a sleep
pdisorder.)
i
c
s

M: PSO/PSI mepr dsrd (o, p, m, p, a, proc,

d, s), sysi/epon, drug(N5A/5B/5C/6A/6B/6D)
spvo

M: anat(s,m,p,4,e,b,d,c,a,f,l,g)/p noco(m,d,e,h,v,s)/cong/tumr, proc,drug(N1A/2AB/C/3/4

C hys/devp/cell sysi/epon,injr /7A/B/C/D)
NS
 [show]
v•d•e
Developmental disorders: Dyslexia and related specific developmental
disorders (F80-F83, 315)

GSpeech and
elanguage/ Expressive language disorder · Aphasia/Dysphasia (Expressive aphasia,
ncommunicationReceptive aphasia) · Landau–Kleffner syndrome · Lisp · Mixed
edisorders receptive-expressive language disorder
r
aScholastic
lskills/ Dyslexia (Alexia (acquired dyslexia), Developmental dyslexia) ·
Dysgraphia (Disorder of written expression) · Dyscalculia (Gerstmann
learning
cdisorder syndrome)
o
nMotor function Developmental dyspraxia
d
iOther Auditory processing disorder · Scotopic sensitivity syndrome
t
i
o
n
s

R
e
l
a
t
e
Dyslexia research · Management of dyslexia/Dyslexia interventions · Reading
d
acquisition · Writing system · Spelling · Literacy · Irlen filters · Recording for the Blind
& Dyslexic · Neuropsychology
t
o
p
i
c
s

L
i
sLanguages by Writing System · People with dyslexia · Dyslexia in fiction
t
s

M: PSO/PSI mepr dsrd (o, p, m, p, a, proc,

d, s), sysi/epon, drug(N5A/5B/5C/6A/6B/6D)
spvo
 [show]
v•d•e
Developmental disorders: Pervasive developmental disorders and autism
spectrum (F84, 299)

M
aCauses · Comorbid conditions · Epidemiology · Heritability · Sociological and cultural
iaspects · Therapies
n

D
i
a
g
Autism spectrum (Asperger syndrome, Autism/High-functioning autism, PDD-NOS) ·
n
Childhood disintegrative disorder · Rett syndrome
o
s
e
s

R
e
l
a
t
e
d

c
ADHD · Anxiety disorder · Epilepsy · Fragile X syndrome · Mental retardation
o
n
d
i
t
i
o
n
s

C
o
n
t
r
o
vAutism rights movement · Autistic enterocolitis · MMR vaccine · Thiomersal (Chelation)
e
r
s
i
e
s
D
i
a
g
n
o
s
tGilliam Asperger's Disorder Scale · Autism Diagnostic Observation Schedule · Autism
iDiagnostic Interview-Revised · Autism Spectrum Quotient · Childhood Autism Rating
cScale

s
c
a
l
e
s

L
i
sAutism-related topics · Fictional characters · People · Speculated historical figures
t
s

M: PSO/PSI mepr dsrd (o, p, m, p, a, proc,

d, s), sysi/epon, drug(N5A/5B/5C/6A/6B/6D)
spvo

[show]
v•d•e
Emotional and behavioral disorders (F90-F98, 312–314)

EADHD · Conduct disorder (ODD) · emotional disorder (Separation anxiety disorder) ·

msocial functioning (Selective mutism, RAD, DAD) · Tic disorder (Tourette syndrome) ·
oSpeech (Stuttering, Cluttering) · Movement disorder (Stereotypic) · Nose-picking · Nail
tbiting
i
o
n
a
l

a
n
d

b
e
h
a
v
i
o
r
a
l

M: PSO/PSI mepr dsrd (o, p, m, p, a, proc,

d, s), sysi/epon, drug(N5A/5B/5C/6A/6B/6D)
spvo

[show]
v•d•e
Attention-deficit hyperactivity disorder (F90, 314)

M
a
i
n

aHistory of ADHD · ADHD in adults · ADHD controversies · ADHD management · List

rof ADHD organizations · Social construct theory of ADHD · ADHD coaching
tMajor characteristics: Attention · Hyperactivity · Impulsivity
i
c
l
e
s

S
u
b
-
ADHD predominantly inattentive (ADHD-I, formerly ADD) · ADHD predominantly
t
hyperactive (ADHD-H, formerly ADHD) · ADHD combined type (ADHD-C)
y
p
e
s

N
Driven to Distraction (1994) · Delivered from Distraction (2005)
o
t
a
b
l
e

P
u
b
l
i
c
a
t
i
o
n
s

N
o
t
a
b
l
e
Russell Barkley · Stephen Faraone · Edward Hallowell · John Ratey · Joseph
Biederman · 19th Century: Alexander Crichton
E
x
p
e
r
t
s

R
e
l
e
v
a
nmethylphenidate (Ritalin) · dextroamphetamine (Dexedrine) · mixed amphetamine salts
t(Adderall) · Non-stimulant: Atomoxetine (Strattera) · More...

D
r
u
g
s

O
tLow arousal theory · Sluggish cognitive tempo · Sensory integration dysfunction ·
hHypokalemic sensory overstimulation · Deficits in Attention, Motor control and
ePerception
r

M: PSO/PSI mepr dsrd (o, p, m, p, a, proc,

d, s), sysi/epon, drug(N5A/5B/5C/6A/6B/6D)
spvo
 [show]
v•d•e
Topics related to Tourette syndrome (F95.2, 307.23)

M
a
Causes and origins · History · Sociological and cultural aspects · Treatment
i
n

T
e
Coprolalia · Copropraxia · Echolalia · Echopraxia · Palilalia · PANDAS · Sensory
r
phenomena · Tic · Tic disorder · Tourettism
m
s

H
i
s
Jean-Martin Charcot · Georges Gilles de la Tourette · Jean Marc Gaspard Itard · Arthur
t
K. Shapiro
o
r
y

O
r
g
a
n
i
Tourette Syndrome Association · Tourette Syndrome Foundation of Canada · Tourettes
z
Action
a
t
i
o
n
s

M
e
I Have Tourette's but Tourette's Doesn't Have Me · John's Not Mad · "Le Petit
d
Tourette" · Maze · Motherless Brooklyn · Quit It · The Tic Code
i
a

NMahmoud Abdul-Rauf · Howard Ahmanson, Jr · Basshunter · Pete Bennett · Brad

oCohen · Jim Eisenreich · Tim Howard · Samuel Johnson · André Malraux · Tobias
tPicker · Nick van Bloss · Michael Wolff
a
b
l
e

p
e
o
p
l
e

M: PSO/PSI mepr dsrd (o, p, m, p, a, proc,

d, s), sysi/epon, drug(N5A/5B/5C/6A/6B/6D)
spvo
Retrieved from "http://en.wikipedia.org/wiki/ICD-
10_Chapter_V:_Mental_and_behavioural_disorders"
Categories: Medical manuals
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