User:Rich Farmbrough/temp68
- ICD 10 2008 (French) http://apps.who.int/classifications/icd10/browse/2008/fr#/T15-T19
- ICD 10 2010 (Eng) apps.who.int/classifications/icd10/browse/2010/en#/T14.0
- http://www.archive.today/4fJ7w[dead link] ICDLS D
- http://www.archive.today/JQ4uq[dead link] ICDLS E
- CDC http://www.cdc.gov/nchs/data/dvs/2e_volume1_2013.pdf
Note: repeating lines are from the original data. They appear represent the normalisation of valid variants.
A
[edit]- A06.700: Amoebiasis, cutaneous
- A06.700: Cutaneous amebiasis
- A06.810: Amoebic balanitis
- A06.810: Balanitis, amoebic
- A18.410: Abscess, tuberculous
- A18.410: Tuberculosis cutis primaria
- A18.420: Lupus vulgaris
- A18.422: Lupus vulgaris tumidus
- A18.424: Tuberculous ulcer
- A18.430: Lupus mutilans
- A18.440: Tuberculosis, warty
- A18.450: Tuberculosis fungosa serpiginosa
- A18.460: Tuberculous ulcer, metastatic
- A18.462: Scrofuloderma
- A18.462: Tuberculosis cutis colliquativa
- A18.470: Tuberculide
- A18.472: Nodular tuberculide
- A18.472: Tuberculide, nodular
- A18.476: Papulonecrotic tuberculide
- A18.476: Tuberculide, papulonecrotic
- A18.480: Erythema nodosum due to tuberculosis
- A18.482: Bazin's disease
- A18.482: Erythema induratum due to tuberculosis
- A18.484: Lichen scrofulosorum
- A18.486: Tuberculous gumma
- A18.490: Tuberculosis, cutaneous
- A21.900: Tularaemia, cutaneous involvement
- A22.000: Anthrax, cutaneous
- A22.000: Anthrax, cutaneous
- A22.000: Malignant pustule
- A23.900: Brucellosis of skin
- A24.300: Melioidosis of the skin
- A25.000: Rat-bite fever, Spirillum minor
- A25.000: Sodoku
- A25.110: Haverhill fever
- A25.110: Rat-bite fever, streptobacillary
- A25.110: Streptobacillary rat-bite fever
- A26.000: Erysipeloid
- A27.010: Canicola fever
- A27.010: Leptospirosis icterohaemorrhagica
- A27.010: Weil's disease
- A27.900: Leptospirosis, cutaneous involvement
- A28.010: Pasteurella multocida infection, cutaneous involvement
- A28.100: Cat scratch fever (Bartonella henselae)
- A28.110: benign Lymphoreticulosis
- A28.110: Lymphoreticulosis, benign
- A30.000: Leprosy, indeterminate
- A30.100: Leprosy, tuberculoid
- A30.200: Leprosy, borderline tuberculoid
- A30.200: Leprosy, borderline tuberculoid
- A30.300: Leprosy, midborderline
- A30.400: Leprosy, borderline lepromatous
- A30.400: Leprosy, borderline lepromatous
- A30.500: Leprosy, lepromatous
- A30.510: Diffuse lepromatous leprosy
- A30.810: Leprosy, dimorphic
- A30.820: Erythema nodosum leprosum
- A30.830: Leprosy, Lucio
- A30.830: Lucio leprosy
- A30.840: Lucio phenomenon
- A30.870: Lepra reaction type 1
- A30.872: Lepra reaction type 1, upgrading
- A30.874: Lepra reaction type 1, downgrading
- A30.900: Hansen's disease
- A30.900: Leprosy, NOS
- A31.110: Fish tank granuloma
- A31.110: Granuloma, fish tank
- A31.110: Granuloma, swimming pool
- A31.110: Mycobacterium marinum infection of skin
- A31.120: Buruli ulcer
- A31.120: Mycobacterium ulcerans infection of skin
- A31.810: Atypical mycobacterium infection, NOS
- A32.000: Listeriosis, cutaneous involvement
- A36.300: Diphtheria, cutaneous
- A38.x00: Scarlet fever
- A38.x00: Scarlet fever
- A41.820: Janeway lesions
- A41.910: Septicaemia affecting skin
- A42.200: Actinomycosis, cervico-facial
- A42.810: Actinomycetoma from Other Actinomycetes
- A42.900: Actinomycosis, NOS
- A43.100: Nocardiosis, cutaneous
- A44.000: Oroya fever, cutaneous involvement
- A44.110: Verruga peruana
- A44.800: Carrion's disease
- A44.850: Bacillary angiomatosis (Bartonella henselae/quintana)
- A44.900: Bartonellosis (Bartonella bacilliformis)
- A46.x00: Erysipelas
- A46.x20: Erysipelas, facial
- A46.x40: Erysipelas of lower limb
- A48.300: Toxic shock syndrome
- A48.300: Toxic shock syndrome
- A48.810: Rhinoscleroma
- A48.820: Rhodoccocus infection
- A48.830: Pseudomonas aeruginosa infection, cutaneous
- A50.900: Congenital syphilis
- A51.000: Syphilitic chancre, genital
- A51.010: Syphilis, primary chancre
- A51.010: Syphilis, primary chancre
- A51.090: Syphilitis, primary
- A51.100: Syphilitic chancre, perianal
- A51.200: Syphilitic chancre, extragenital
- A51.210: Syphilis, primary chancre
- A51.300: Syphilis, secondary
- A51.302: Macular syphilide
- A51.304: Papular syphilide
- A51.306: Nodular syphilide
- A51.308: Psoriasiform syphilide
- A51.310: Syphilide, macular
- A51.312: Condylomata lata
- A51.320: Secondary syphilis, oral mucous membrane lesions
- A51.330: Syphilitic alopecia
- A51.350: Secondary syphilis, tonsillitis
- A51.360: Leucoderma syphiliticum
- A51.382: Syphilis, secondary - nail involvement
- A51.390: Secondary Syphilis
- A52.100: Neurosyphilis, symptomatic
- A52.200: Neurosyphilis, asymptomatic
- A52.300: Neurosyphilis, NOS
- A52.720: Gumma, syphilitic
- A52.900: Syphilis, late
- A53.000: Latent syphilis
- A53.900: Syphilis
- A54.000: Gonococcal infection of lower genitourinary tract
- A54.020: Gonococcal cervicitis
- A54.030: Gonococcal urethritis
- A54.040: Gonococcal cystitis
- A54.050: Gonococcal vulvovaginitis
- A54.110: Gonococcal bartholinitis
- A54.300: Gonococcal infection of eye
- A54.400: Gonococcal infection of musculoskeletal system
- A54.500: Gonococcal pharyngitis
- A54.800: Gonococcal infection, other
- A54.820: Fitz-Hugh-Curtis syndrome
- A54.850: Gonococcal septicaemia affecting skin
- A54.900: Gonorrhoea, NOS
- A55.x00: Lymphogranuloma inguinale
- A56.000: Urethritis, chlamydial
- A56.020: Cervicitis, chlamydial
- A56.030: Salpingitis, chlamydial
- A57.x00: Chancroid
- A58.x00: Donovanosis
- A58.x00: Granuloma inguinale
- A59.000: Trichomoniasis, urogenital
- A60.010: Herpes simplex, genital
- A60.100: Herpes simplex, perianal
- A63.000: Condylomata acuminata
- A64.x00: Venereal disease, NOS
- A65.x00: Bejel
- A65.x00: Syphilis, endemic non-venereal
- A66.000: Primary yaws
- A66.000: Yaws, primary
- A66.110: Papillomata, multiple of yaws
- A66.200: Early skin lesions of yaws, other
- A66.300: Hyperkeratosis of yaws
- A66.500: Gangosa
- A66.500: Gangosa
- A66.710: Mucosal yaws
- A66.900: Pian in yaws
- A66.900: Yaws
- A66.900: Yaws
- A67.000: Pinta, early
- A67.100: Pintids
- A67.200: Pinta, late phase
- A67.900: Pinta
- A68.900: Relapsing fever, unspecified
- A69.000: Stomatitis gangrenosa
- A69.010: Cancrum oris
- A69.020: Cancrum oris
- A69.020: Noma
- A69.110: Angina, Vincent's
- A69.120: Gingivitis, acute necrotising ulcerative
- A69.200: Lyme disease
- A69.210: Borrelia burgdorferi infection
- A69.220: Erythema chronicum migrans
- A69.230: Lymphocytoma cutis
B
[edit]- B00.000: Eczema herpeticum
- B00.100: Herpes simplex infection
- B00.110: Herpes simplex labialis
- B00.210: Herpes simplex gingivostomatitis
- B00.215: Stomatitis, aphthous
- B00.216: Stomatitis, herpetiform
- B00.500: Herpes simplex, primary ocular
- B00.530: Herpetic keratitis
- B00.550: Herpes simplex keratoconjunctivitis
- B00.700: Herpes simplex, disseminated
- B00.800: Herpes simplex, other
- B00.840: Herpetic whitlow
- B01.900: Chickenpox
- B01.990: Herpesvirus varicellae infection (chickenpox)
- B02.210: Herpes zoster oticus
- B02.270: Ramsay-Hunt syndrome
- B02.300: Herpes zoster infection, ophthalmic
- B02.700: Herpes zoster, disseminated
- B02.910: Herpes zoster
- B03.x00: Smallpox
- B03.x20: Smallpox
- B04.x00: Monkeypox
- B05.990: Measles
- B05.990: Morbilli
- B06.900: Rubella
- B06.990: Rubella
- B06.990: Rubella
- B07.x00: Common warts
- B07.x10: Filiform warts
- B07.x12: Warts, hand
- B07.x14: Plantar warts
- B07.x18: Mosaic plantar warts
- B07.x18: Mosaic plantar warts
- B07.x20: Warts, plane
- B07.x30: Butcher's warts
- B07.x30: Butcher's warts
- B08.010: Cowpox
- B08.030: Cowpox
- B08.040: Ecthyma contagiosum
- B08.040: Orf
- B08.050: Vaccinia
- B08.100: Molluscum contagiosum
- B08.200: Roseola infantum
- B08.200: Exanthema subitum
- B08.300: Fifth disease
- B08.300: Erythema infectiosum
- B08.400: Hand, foot and mouth disease
- B08.500: Herpangina
- B08.820: Foot and mouth disease
- B08.830: Tanapox
- B09.x20: Viral exanthem
- B20.010: Tuberculosis in HIV disease
- B20.100: HIV-modified bacterial infection of skin (elsewhere classified)
- B20.110: Bacillary angiomatosis in HIV disease
- B20.200: Cytomegalovirus infection in HIV disease
- B20.300: HIV-modified viral infection of skin (elsewhere classified)
- B20.400: HIV-modified candidosis (elsewhere classified)
- B20.500: HIV-modified fungal infection of skin (elsewhere classified)
- B20.800: HIV disease resulting in other infectious or parasitic infections
- B20.900: HIV-modified infection/infestation of skin, NOS
- B21.100: Burkitt's lymphoma in HIV disease
- B21.200: HIV disease with non-Hodgkin's lymphoma, other
- B21.300: HIV-associated cutaneous lymphoma (elsewhere classified)
- B21.800: HIV disease with malignant neoplasm, other
- B21.900: HIV disease with malignant neoplasm, NOS
- B22.000: HIV disease resulting in encephalopathy
- B22.010: Dementia in HIV disease
- B22.200: Slim disease
- B22.700: HIV disease resulting in multiple diseases, elsewhere classified
- B23.000: Acute HIV infection syndrome
- B24.x20: Human immunodeficiency virus infection
- B24.x20: Acquired immune deficiency syndrome
- B24.x90: Human immunodeficiency virus infection
- B25.810: Cytomegalovirus infection of skin
- B27.010: Epstein-Barr virus infection
- B27.800: Infectious mononucleosis
- B33.100: Ross River virus infection
- B35.006: Tinea capitis
- B35.020: Kerion (due to tinea elsewhere classified)
- B35.020: Kerion
- B35.030: Favus
- B35.040: Tinea barbae
- B35.040: Beard ringworm
- B35.050: Tinea barbae
- B35.060: Tinea faciei
- B35.100: Tinea unguium
- B35.100: Onychomycosis due to dermatophyte
- B35.110: Total dystrophic onychomycosis
- B35.110: Onychomycosis, total dystrophic
- B35.120: Onychomycosis, distal and lateral subungual
- B35.130: Onychomycosis, proximal subungual
- B35.140: Superficial white onychomycosis
- B35.190: Onychomycosis
- B35.200: Tinea manuum
- B35.200: Hand ringworm
- B35.300: Foot ringworm
- B35.300: Tinea pedis
- B35.310: Interdigitale tinea pedis
- B35.330: Moccasin foot
- B35.400: Tinea corporis
- B35.400: Ringworm of body
- B35.500: Tokelau
- B35.500: Tinea imbricata
- B35.600: Tinea cruris
- B35.610: Ringworm of groin
- B35.810: Tinea profunda
- B35.820: Granulomatous dermatophytosis
- B35.830: Majocchi's granuloma
- B35.890: Disseminated dermatophytosis
- B35.900: Tinea, NOS
- B35.900: Ringworm, NOS
- B36.000: Pityriasis versicolor
- B36.000: Tinea versicolor
- B36.100: Tinea nigra
- B36.100: Keratomycosis nigricans palmaris
- B36.200: White piedra
- B36.200: Trichosporosis, white
- B36.200: Piedra alba
- B36.300: Trichomycosis nodularis, black
- B36.300: Trichosporosis, black
- B36.810: Folliculitis, malassezia (pityrosporum)
- B36.810: Malassezia (pityrosporum) folliculitis
- B36.820: Onychomycosis due to mould infection
- B36.900: Dermatomycosis, NOS
- B36.920: Otomycosis, NOS
- B37.000: Oral candidiasis
- B37.000: Stomatitis, candidal
- B37.000: Candidosis, oral
- B37.000: Candidosis, oral
- B37.010: Chronic atrophic candidiasis
- B37.020: Chronic hyperplastic candidiasis
- B37.030: Candida leukoplakia
- B37.050: Perlèche moniliasis
- B37.050: Angular cheilitis, candidal
- B37.210: Candidiasis, cutaneous
- B37.212: Candidosis, disseminated cutaneous
- B37.214: Candidosis, flexural
- B37.216: Erosio interdigitalis blastomycetica
- B37.216: Candidiasis, interdigital
- B37.220: Nail candidiasis
- B37.220: Candidiasis, nail
- B37.230: Candidal paronychia
- B37.230: Paronychia due to candidiasis
- B37.250: Cutaneous candidal granuloma
- B37.260: Candidiasis, granulomatous
- B37.280: Chronic mucocutaneous candidiasis
- B37.290: Candidosis, chronic mucocutaneous
- B37.290: Candidiasis, chronic mucocutaneous
- B37.310: Candidiasis of vulva
- B37.310: Vulvar candidiasis
- B37.330: Candida vulvovaginitis
- B37.330: Candida vulvovaginitis
- B37.410: Candida balanitis
- B37.410: Candida balanitis
- B37.700: Candida septicaemia
- B37.885: Candidal cheilitis
- B37.885: Cheilitis, candidal
- B37.900: Thrush
- B37.900: Candidosis
- B37.900: Moniliasis, NOS
- B37.900: Candidiasis, NOS
- B38.300: Coccidioidomycosis, cutaneous
- B39.300: Histoplasmosis, disseminated cutaneous
- B39.400: American histoplasmosis, NOS
- B39.500: Histoplasmosis, African
- B39.900: Histoplasmosis, NOS
- B40.300: Blastomycosis, cutaneous
- B40.900: Gilchrist's disease
- B41.810: Paracoccidioidomycosis of skin
- B41.900: Paracoccidioidomycosis, NOS
- B41.900: Lutz Splendore Almeida disease
- B42.100: Sporotrichosis, lymphatic cutaneous
- B43.000: Chromoblastomycosis of skin
- B43.000: Chromomycosis of skin
- B43.000: Verrucous dermatitis
- B43.900: Chromoblastomycosis
- B44.810: Otomycosis due to aspergillus spp.
- B45.200: Cutaneous cryptococcosis
- B45.200: Cryptococcosis of skin
- B46.100: Mucormycosis, rhinocerebral
- B46.100: Rhinocerebral mucormycosis
- B46.300: Mucormycosis of skin
- B46.300: Cutaneous mucormycosis
- B46.310: Subcutaneous mucormycosis
- B46.310: Mucormycosis, subcutaneous
- B46.810: Entomophthoromycosis
- B46.900: Zygomycosis, NOS
- B47.000: Eumycetoma
- B47.000: Maduromycosis
- B47.010: Madura foot, mycotic
- B47.900: Mycetoma of foot, NOS
- B47.910: Madura foot, NOS
- B48.000: Lobomycosis
- B48.100: Rhinosporidiosis
- B48.400: Disseminated cutaneous mycosis due to Penicillium spp.
- B48.810: Alternariosis, cutaneous
- B49.x00: Mycosis, NOS
- B49.x00: Fungus infection of skin
- B55.000: Kala azar
- B55.000: Leishmaniasis, visceral affecting skin
- B55.010: Leishmaniasis, post kala azar dermal
- B55.010: Leishmaniasis, post kala-azar dermal
- B55.010: Post-kala-azar dermal leishmaniasis
- B55.100: Oriental sore
- B55.100: Delhi boil
- B55.100: Cutaneous leishmaniasis, NOS
- B55.110: Leishmaniasis of skin diffuse
- B55.130: Lupoid leishmaniasis
- B55.130: Leishmaniasis, lupoid
- B55.200: Leishmaniasis, American mucocutaneous
- B55.200: American cutaneous leishmaniasis
- B55.200: Espundia
- B55.900: Leishmaniasis, NOS
- B56.000: Trypanosomiasis Gambiense
- B56.100: Rhodesiense trypanosomiasis
- B56.900: Trypanosomiasis African, NOS
- B56.910: Sleeping sickness, NOS
- B57.510: Chagoma
- B57.510: Chagas disease skin
- B58.810: Toxoplasmosis of skin
- B58.900: Toxoplasmosis, NOS
- B56.000: Trypanosomiasis Gambiense
- B56.100: Rhodesiense trypanosomiasis
- B56.900: Trypanosomiasis African, NOS
- B56.910: Sleeping sickness, NOS
- B57.510: Chagas disease skin
- B57.510: Chagoma
- B58.810: Toxoplasmosis of skin
- B58.900: Toxoplasmosis, NOS
- B65.210: Katayama disease
- B65.300: Cercarial dermatitis
- B65.300: Dermatitis, cercarial
- B65.300: Dermatitis, schistosome
- B65.300: Schistosomiasis of skin
- B65.300: Sea bather's eruption
- B65.300: Swimmer's itch
- B65.900: Bilharziasis, NOS
- B65.900: Schistosomiasis of skin
- B67.900: Echinococcosis of skin
- B68.900: Tapeworm, dermatosis due to
- B69.810: Cysticercosis of skin
- B69.900: Cysticercosis of skin
- B70.100: Sparganosis of skin
- B70.110: Sparganosis of skin
- B72.x00: Dracunculosis
- B73.x00: Onchocerciasis
- B73.x10: Onchodermatitis
- B73.x30: Onchocerciasis
- B74.000: Filariasis due to wuchereria bancrofti
- B74.010: Elephantiasis, filarial
- B74.100: Filariasis due to brugia malayi
- B74.300: Loa loa
- B74.300: Loiasis
- B74.410: Mansonelliasis of skin
- B74.900: Filariasis
- B75.x00: Trichinosis
- B75.x00: Trichinosis
- B76.000: Ancylostomiasis of skin
- B76.900: Disease, hookworm
- B76.900: Hookworm infestation, NOS
- B76.910: Creeping eruption
- B76.910: Cutaneous larva migrans
- B76.910: Eruption, creeping
- B76.910: Larva migrans
- B76.910: Larva migrans
- B77.900: Acariasis
- B78.100: Strongyloidiasis affecting skin
- B78.110: Larva currens (strongyloidiasis)
- B78.700: Strongyloidiasis, disseminated
- B78.900: Strongyloidiasis, NOS
- B80.x00: Oxyuriasis
- B83.000: Larva migrans, visceral
- B83.000: Visceral larva migrans
- B83.010: Toxocariasis
- B83.100: Gnathostomiasis
- B85.000: Head lice
- B85.000: Lice, head
- B85.000: Pediculosis capitis
- B85.100: Body lice
- B85.100: Lice, body
- B85.100: Pediculosis corporis
- B85.100: Vagabond's disease
- B85.200: Pediculosis, NOS
- B85.300: Crabs
- B85.300: Lice, pubic
- B85.300: Phthiriasis pubis
- B85.300: Pubic lice
- B85.310: Maculae caeruleae (phthiriasis)
- B85.310: Taches bleuâtres (phthiriasis)
- B85.400: Pediculosis with phthiriasis
- B85.400: Phthiriasis with pediculosis
- B86.x00: Scabies, human
- B86.x10: Scabies, Norwegian
- B86.x20: Post-scabietic nodules
- B86.x30: Post-scabietic eczema
- B87.000: Myiasis of skin
- B87.010: Myiasis, creeping
- B87.100: Myiasis of wound
- B87.100: Wound myiasis
- B87.900: Myiasis
- B88.010: Dermatosis due to plant mites
- B88.010: Harvest itch
- B88.010: Trombiculosis
- B88.020: Demodicidosis
- B88.030: Trombiculosis
- B88.040: Cheyletiella dermatitis
- B88.050: Animal scabies
- B88.050: Dermatosis due to animal mites
- B88.060: Dermatosis due to bird mites
- B88.100: Tungiasis
- B88.300: Leech bite
- B88.820: Tick bite
- B88.830: Protothecosis of skin
C
[edit]- C02.910: Squamous cell carcinoma of tongue
- C06.910: Verrucous carcinoma of oral cavity
- C25.410: Glucagonoma syndrome
- C43.992: Malignant melanoma, mucosal
- C43.994: Malignant melanoma, extracutaneous
- C43.L10: Malignant melanoma, nodular
- C43.L20: Malignant melanoma, superficial spreading
- C43.L40: Malignant melanoma, lentigo maligna
- C43.L50: Malignant melanoma, amelanotic
- C43.L60: Malignant melanoma, acral lentiginous
- C43.L80: Malignant melanoma, histological type unclassifiable
- C43.L82: Blue naevus, malignant
- C43.L90: Malignant melanoma, clinical & histological type unspecified
- C44.L12: Marjolin's ulcer
- C44.L21: Basalioma
- C44.L21: Basal cell carcinoma
- C44.L24: Basal cell carcinoma, micronodular
- C44.L25: Basal cell carcinaoma, superficial
- C44.L26: Basal cell carcinoma, nodualr
- C44.L26: Basal cell carcinoma, circumscribed solid
- C44.L27: Basal cell carcinoma, cystic
- C44.L28: Basal cell carcinoma, morphoeic
- C44.L30: Basal cell carcinoma, adenoid
- C44.L32: Basal cell carcinoma, nodulo-ulcerative
- C44.L33: Basal cell carcinoma, pigmented
- C44.L34: Basal cell carcinoma, keratotic
- C44.L35: Ulcus, rodent
- C44.L38: Basal cell carcinoma, recurrent
- C44.L40: Spiradenoma, malignant
- C44.L42: Cylindroma, malignant
- C44.L43: Sweat gland carcinoma, NEC
- C44.L44: Merkel cell carcinoma
- C44.L45: Pilomatrixoma, malignant
- C44.L46: Sebaceous carcinoma
- C44.L47: Trichilemmal carcinoma
- C44.L48: Squamous cell carcinoma
- C44.L56: Squamous cell carcinoma, verrucous
- C44.L62: Apocrine adenocarcinoma
- C44.L64: Eccrine spiradenoma, malignant
- C44.L67: Porocarcinoma, eccrine
- C44.L67: Eccrine porocarcinoma
- C44.L67: Hidradenocarcinoma
- C44.L68: Sweat gland tumour, malignant
- C44.L75: Paget's disease, extramammary
- C44.L79: Fibroepithelioma of Pinkus
- C46.010: Kaposi's sarcoma in HIV disease
- C46.010: Kaposi's sarcoma
- C46.020: Kaposi's sarcoma, sporadic
- C46.030: Kaposi's sarcoma, endemic
- C46.900: Kaposi's sarcoma, NOS
- C47.900: Nerve sheath-derived malignant neoplasm (NEC/NOS)
- C47.910: Granular cell tumour, malignant
- C49.M10: Histiocytoma, malignant fibrous
- 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
- C50.010: Paget's disease of nipple
- C50.810: Cancer en cuirasse
- C51.910: Malignant melanoma of vulva
- C60.910: Carcinoma of penis
- C60.910: Penile carcinoma
- C62.920: Seminoma
- C62.930: Teratoma
- C77.801: Lymph node matastasis due to melanoma
- C77.900: Lymph node metastasis, NOC
- C77.930: Lymph node matastasis due to SCC
- C78.810: Visceral metastasis due to melanoma
- C79.210: Metastasis in skin, NOS
- C79.240: Intransit metastasis in skin, due to melanoma
- C80.x20: Erysipelas carcinomatosum
- C81.900: Hodgkin's disease, NOS
- C81.900: Hodgkin's disease affecting the skin
- C83.310: Sarcoma, reticulum cell
- C83.410: Immunoblastic lymphoma
- C83.700: Burkitt's lymphoma
- C83.900: Diffuse non-Hodgkin's lymphoma, NOS
- C84.000: Mycosis fungoides
- C84.002: Premycotic eruption
- C84.004: Mycosis fungoides, patch
- C84.006: Cutaneous T-cell lymphoma, patch/plaque stage
- C84.006: Mycosis fungoides, patch/plaque stage
- C84.008: Cutaneous T-cell lymphoma, erythrodermic
- C84.008: Mycosis fungoides, erythrodermic
- C84.010: Poikilodermatous mycosis fungoides
- C84.010: Mycosis fungoides, poikilodermatous
- C84.012: Mycosis fungoides, tumour stage
- C84.014: Mycosis fungoides, "tumeur d'emblée" type
- C84.018: Cutaneous T-cell lymphoma , follicular mucinosis type
- C84.018: Follicular mucinosis (T cell lymphoma)
- C84.018: Mycosis fungoides, follicular mucinosis type
- C84.030: Woringer-Kolopp disease (pagetoid reticulosis)
- C84.030: Pagetoid reticulosis
- C84.040: Ketron-Goodman disease (pagetoid reticulosis)
- C84.040: Pagetoid reticulosis, generalised
- C84.050: Slack skin disease, granulomatous
- C84.050: Granulomatous slack skin disease
- C84.060: Cutaneous T-cell lymphoma, panniculitis-like
- C84.100: Sézary syndrome
- C84.200: T-cell lymphoma, T-zone (involving skin)
- C84.300: T-cell lymphoma, Lennert's (involving skin)
- C84.300: Lennert's lymphoma
- C84.400: Peripheral T cell lymphoma
- C84.412: Peripheral T cell lymphoma, pleomorphic
- C84.414: T-cell lymphoma, pleomorphic small/medium-sized cell cutaneous
- C84.418: T-cell lymphoma, CD-30 positive anaplastic large cell cutaneous
- C84.420: CD-30 positive anaplastic large T-cell cutaneous lymphoma
- C84.420: Ki-1 positive T cell lymphoma
- C84.422: T-cell lymphoma, CD-30 positive pleomorphic large T-cell cutaneous
- C84.424: T-cell lymphoma, CD-30 negative pleomorphic large cell cutaneous
- C84.426: T-cell lymphoma, CD-30 positive T-immunoblastic cutaneous
- C84.430: Ki-1 positive T cell lymphoma
- C84.430: Malignant lymphoma, CD-30 positive large T-cell cutaneous
- C84.460: Angioimmunoblastic lymphadenopathy
- C84.500: T-cell lymphoma involving skin (NEC/NOS)
- C85.100: B-cell lymphoma (NEC/NOS) with skin involvement
- C85.110: B-cell lymphoma, small lymphocytic (involving skin)
- C85.900: Lymphoma, NOS
- C88.000: Macroglobulinemia Waldenström
- C88.000: Waldenström's macroglobulinemia
- C90.002: Myelomatosis
- C90.002: Multiple myeloma, cutaneous infiltration by
- C90.010: Kahler's disease
- C90.100: Plasma cell leukemia
- C90.200: Myeloma solitary
- C90.201: Plasmocytoma, cutaneous
- C90.201: Cutaneous plasmacytoma
- C91.100: T-cell leukaemia, chronic lymphocytic (involving skin)
- C91.400: Hairy-cell leukaemia (involving skin)
- C91.401: Leukemic reticuloendotheliosis
- C91.500: Adult T-cell lymphoma-leukaemia (ATLL)
- C92.100: Chronic myeloid leukaemia : leukaemic infiltration of skin
- C92.700: Myeloid leukaemia : leukaemic infiltration of skin
- C93.700: Monocytic leukaemia : leukaemic infiltration of skin
- C95.900: Leukaemic infiltration of skin
- C96.000: Letterer-Siwe disease
- C96.110: Histiocytic medullary reticulosis
- C96.120: Malignant histiocytosis (involving skin)
- C96.200: Mastocytosis, malignant
- C96.210: Mastocytosis, malignant
D
[edit]- D03.L00: Malignant melanoma, in situ
- D03.L10: Lentigo maligna
- D04.L10: Bowen´s disease
- D07.110: Erythroplasia of Queyrat of vulva
- D07.120: Vulval intraepithelial neoplasia (VIN)
- D07.410: Erythroplasia of Queyrat, penis
- D10.120: Abrikosoff´s tumour of tongue
- D10.310: White sponge nevus
- D17.910: Lipoma
- D17.920: Lipomata, multiple
- D17.930: Angiolipoma
- D17.940: Lipoblastomatosis
- D17.950: Hibernoma
- D18.010: Haemangioma
- D18.010: Angioma, NOS
- D18.011: Glomus tumour(s)
- D18.011: Glomus tumour
- D18.013: Angioma senile
- D18.014: Cavernous haemangioma
- D18.015: Haemangioma, capillary
- D18.015: Capillary angioma
- D18.016: Multiple progressive angiomatosis
- D18.050: Hemangioma, venous
- D18.050: Venous lake
- D18.100: Lymphangioma
- D18.110: Lymphangioma, simple
- D18.130: Lymphangioma circumscriptum cutis
- D18.130: Lymphangioma circumscriptum
- D18.140: Lymphangioma, cavernous
- D18.140: Cystic hygroma
- D18.140: Hygroma, cystic
- D21.M20: Masson´s pseudoangiosarcoma
- D21.M30: Synovioma, giant-cell
- D21.M40: Leiomyoma
- D21.M50: Rhabdomyoma
- D21.M60: Angioleiomyoma
- D22.301: Naevus of Ota
- D22.301: Ota's naevus
- D22.504: Naevus of Ito
- D22.505: Mongolian spot
- D22.L14: Naevus, compound
- D22.L22: Naevus, dermal cellular
- D22.L30: Spindle cell naevus of Reed
- D22.L32: Naevus, Spitz
- D22.L32: Naevus, desmoplastic Spitz
- D22.L34: Naevus, halo
- D22.L36: Pseudomelanoma
- D22.L42: Naevus, blue
- D22.L42: Blue naevus
- D22.L50: Giant nevus
- D22.L60: Naevus, congenital (NEC/NOS)
- D22.L80: Balloon cell naevus
- D23.L12: Trichilemmoma
- D23.L13: Trichoepithelioma
- D23.L14: Trichoepithelioma, giant solitary
- D23.L15: Trichofolliculoma
- D23.L17: Epithelioma calcificans Malherbe
- D23.L17: Pilomatrixoma
- D23.L18: Trichoadenoma
- D23.L22: Winer's pore
- D23.L24: Trichoblastoma
- D23.L25: Fibrofolliculomas, multiple
- D23.L26: Trichodiscoma
- D23.L27: Eccrine tumour, benign (NEC/NOS)
- D23.L30: Eccrine hidrocystoma
- D23.L31: Hidroacanthoma simplex
- D23.L31: Eccrine poroma
- D23.L32: Eccrine syringofibroadenoma
- D23.L33: Cylindroma
- D23.L36: Apocrine tumour, benign (NEC/NOS)
- D23.L37: Apocrine adenoma, tubular
- D23.L39: Hidrocystoma, apocrine
- D23.L45: Syringomata, eruptive
- D23.L48: Hidradenoma papilliferum
- D23.L49: Spiradenoma
- D23.L53: Fibroma
- D23.L54: Fibroma molle
- D23.L59: Fibroma, periungual
- D23.L62: Dermatofibroma
- D23.L67: Acanthoma fissuratum
- D23.L71: Keratoacanthoma
- D23.L73: Angiokeratoma circumscriptum
- D23.L74: Angiokeratoma of Mibelli
- D23.L75: Angiofibroma
- D23.L79: Osteoma cutis
- D23.L83: Verruciform xanthoma
- D24.x10: Erosive adenomatosis of nipple
- D24.x30: Adenoma of nipple
- D29.010: Pearly penile papules
- D29.010: Hirsuties papillaris penis
- D29.420: Angiokeratoma, scrotal
- D29.430: Dartoic myoma
- D36.110: Neuroma, cutaneous
- D36.150: Nerve sheath-derived benign neoplasm
- D36.150: Neurilemmoma
- D36.160: Neurofibroma
- D36.160: Neurofibroma single
- D36.170: Tumor, granular cell
- D36.170: Abrikossoff's tumour
- D36.170: Granular cell myoblastoma
- D36.170: Granular cell tumour
- D36.180: Ganglioneuroma
- D45.x00: Polycythaemia vera
- D47.200: Gammopathy, monoclonal
- D47.300: Idiopathic hemorrhagic thrombocythemia
- D48.110: Tumour, soft tissue NOS
- D48.510: FAMMM syndrome
- D48.520: Dysplastic nevus syndrome
- D48.520: BK-Mole syndrome, hereditary
- D48.540: Dysplastic nevus
- D48.560: Generalised follicular hamartoma
- D48.570: Desmoid tumour
- D50.110: Paterson Kelly syndrome
- D50.110: Plummer Vinson syndrome
- D59.110: Cold agglutinins
- D61.010: Fanconi syndrome
- D65.x20: Purpura fulminans
- D68.810: Antiphospholipid syndrome
- D68.830: Systemic lupus erythematosus-associated antiphospholipid syndrome
- D68.900: Bruising/purpura due to coagulation disorder (NEC/NOS)
- D69.010: Henoch-Schönlein purpura
- D69.010: Anaphylactoid purpura
- D69.020: Purpura, toxic
- D69.020: Toxic purpura
- D69.030: Allergic vasculitis
- D69.030: Vasculitis, leucocytoclastic
- D69.030: Vasculitis, allergic
- D69.030: Angiitis leucocytoclastic
- D69.030: Leucocytoclastic vasculitis
- D69.030: Gougerot Ruiter disease
- D69.050: Purpura due to drug
- D69.050: Drug-induced purpura
- D69.080: Purpura, idiopathic
- D69.110: Glanzmann Naegeli syndrome
- D69.210: Purpura
- D69.220: Purpura simplex
- D69.230: Auto-erythrocyte sensitisation
- D69.230: Syndrome painful bruising
- D69.230: Gardner Diamond syndrome
- D69.240: Eczematid like purpura
- D69.250: Purpura teleangiectatica arciformis Touraine
- D69.260: Purpura senile
- D69.260: Senile purpura
- D69.270: Steroid-induced purpura
- D69.280: Purpura, contact
- D69.280: Contact purpura
- D69.290: Itching purpura
- D69.300: Purpura, autoimmune thrombocytopenic
- D69.300: Werlhof's disease
- D69.300: Idiopathic thrombocytopenic purpura
- D69.310: Autoimmune thrombocytopenic purpura
- D69.500: Thrombocytopenic purpura, sencondary
- D69.507: Kasabach-Merritt syndrome
- D69.507: Kasabach-Merritt syndrome
- D69.507: Purpura, haemangioma-associated
- D69.507: Haemangiomatosis with thrombocytopenia
- D69.810: Black heel
- D71.x10: Chronic granulomatous disease of childhood
- D72.100: Eosinophilia
- D72.120: Hypereosinophilic syndrome
- D76.000: Langerhans cell histiocytosis
- D76.010: Histiocytosis X, chronic progressive
- D76.020: Hand Schuller Christian disease
- D76.030: Eosinophilic granuloma
- D76.050: Langerhans cell histiocytosis, Hashimoto-Pritzker type
- D76.050: Hashimoto-Pritzker syndrome
- D76.100: Hemophagocytic lymphohistiocytosis
- D76.100: Lymphohistiocytosis, hemophagocytic
- D76.301: Reticulohistiocytic granuloma
- D76.320: Benign cephalic histiocytosis
- D76.330: Familial sky blue histiocytosis
- D76.330: Histiocytosis, familial sea-blue
- D76.340: Histiocytomata, generalised eruptive
- D76.360: Sinus histiocytosis with massive lymphadenopathy
- D76.360: Rosai-Dorfman disease
- D76.370: Plane xanthoma
- D76.380: Xanthogranuloma, necrobiotic
- D76.380: Necrobiotic xanthogranuloma
- D76.390: Juvenile xanthogranuloma
- D81.210: Omenn's syndrome
- D81.900: Immunodeficiency, severe combined
- D82.000: Wiskott-Aldrich syndrome
- D82.100: DiGeorge syndrome
- D82.400: Buckley's syndrome
- D82.400: Hyper-IgE syndrome
- D82.400: Job's syndrome
- D84.100: Complement deficiency (NEC/NOS)
- D84.110: Angioneurotic edema, hereditary
- D84.110: Angio-oedema, hereditary
- D84.112: [[# C1 esterase inhibitor deficiency
- D84.900: Immunodeficiency, NOS
- D86.300: Sarcoidosis, cutaneous
- D86.310: Sarcoidosis, papular
- D86.312: Sarcoidosis, maculopapular
- D86.314: Sarcoidosis, nodular
- D86.316: Sarcoidosis, subcutaneous nodular
- D86.318: Sarcoidosis, annular
- D86.320: Sarcoidosis, plaque
- D86.330: Sarcoidosis in scar
- D86.340: Lupus pernio
- D86.350: Sarcoidosis, acute with erythema nodosum
- D86.360: Angiolupoid
- D86.810: Heerfordt's syndrome
- D86.830: Ostitis multiplex cystoides Jüngling
- D86.920: Besnier Boeck Schaumann disease
- D89.010: Hypergammaglobulinemic purpura
- D89.100: Cryoglobulinemia
- D89.120: Cryofibrinogenemia
E
[edit]- E03.810: Myxedema, diffuse
- E03.900: Hypothyroidism, skin signs of
- E03.910: Myxoedema (hypothyroidism)
- E05.810: Myxedema, pretibial
- E05.900: Hyperthyroidism, NOS
- E1i.500: Diabetic angiopathy
- E1i.501: Diabetic microangiopathy, dermatoses due to
- E1i.504: Neuropathic ulcer due to diabetes
- E1i.505: Gangrene wet of feet in diabetic
- E1i.506: Dermopathy, diabetic
- E1i.506: Diabetic dermopathy
- E1i.507: Rubeosis, diabetic
- E1i.507: Diabetic rubeosis
- E1i.507: Diabetic rubeosis
- E1i.601: Diabetic thick skin
- E1i.604: Necrobiosis lipoidica, diabetic
- E1i.605: Bulla due to diabetes mellitus
- E1i.605: Bullosis diabeticorum
- E1i.606: Cheiroarthropathy, diabetic
- E22.000: Acromegaly
- E23.010: Sheehan's syndrome
- E24.200: Cushing's syndrome, drug-induced
- E24.900: Cushing syndrome, cutaneous signs due to
- E25.900: Adrenogenital syndrome, NOS
- E27.100: Addison's disease, cutaneous signs due to
- E28.200: Stein Leventhal syndrome
- E28.200: Polycystic ovary syndrome, cutaneous manifestations of
- E29.900: Testicular disorder, cutaneous marker of (NEC/NOS)
- E29.920: Hypogonadism
- E30.000: Delayed puberty
- E30.100: Precocious puberty
- E30.100: Precocious puberty
- E34.000: Carcinoid syndrome
- E34.820: Werner's syndrome
- E34.830: Leprechaunism
- E34.840: Progeria
- E34.850: Acrogeria
- E34.860: Progeria infantilis
- E34.860: Hutchinson Gilford syndrome
- E34.870: Metageria
- E34.900: Endocrine disorder, cutaneous marker of (NEC/NOS)
- E40.x00: Kwashiorkor
- E41.x00: Marasmus
- E50.810: Keratosis follicular due to vitamin A deficiency
- E50.820: Xeroderma due to vitamin A deficiency
- E50.830: Hyperkeratosis due to vitamin A deficiency
- E50.830: Phrynoderma
- E52.x00: Pellagra
- E52.x10: Pellagroid
- E53.000: Ariboflavinosis
- E53.000: [[Vitamin # B2 deficiency
- E53.100: [[Vitamin # B6 deficiency
- E53.850: Folate deficiency
- E53.870: [[Deficiency vitamin # B12 with dermatosis
- E54.x00: Scurvy
- E56.100: Vitamin K deficiency
- E60.x00: Zinc deficiency, nutritional
- E60.x10: Zinc depletion syndrome
- E61.100: Iron deficiency, dermatoses associated with
- E66.900: Obesity, NOS
- E67.000: Hypervitaminosis A, skin disease due to
- E67.100: Aurantiasis
- E70.000: Phenylketonuria - PKU
- E70.000: Folling's syndrome
- E70.000: Phenylpyruvic oligophrenia
- E70.100: Hyperphenylalaninemia
- E70.210: Alkaptonuria
- E70.230: Richner-Hanhart oculocutaneous syndrome (tyrosinaemia II)
- E70.230: Ochronosis
- E70.300: Albinism, NOS
- E70.300: Albinism
- E70.310: Oculocutaneous albinism
- E70.312: Albinism, partial
- E70.314: Tyrosinase-positive oculocutaneous albinism (type 2)
- E70.314: Albinism, oculocutaneous type 2 (tyrosinase positive)
- E70.314: Oculocutaneous albinism - tyrosinase-negative (type 1)
- E70.318: Albinoidism
- E70.320: Waardenburg's syndrome
- E70.340: Chediak Higashi syndrome
- E70.340: Oculocutaneous albinism - Chediak-Higashi
- E70.350: Piebaldism
- E70.358: Tietz 's syndrome
- E70.360: Oculocutaneous albinism - Hermansky-Pudlak
- E70.360: Hermansky Pudlak syndrome
- E70.380: Cross syndrome
- E72.020: Hartnup disease
- E72.510: Leg ulcer due to prolidase deficiency
- E75.220: Gaucher's disease
- E75.230: Niemann-Pick disease
- E75.240: Lipogranulomatosis, disseminated
- E75.240: Farber's disease
- E75.240: Lipogranulomatosis disseminated
- E75.250: Angiokeratoma corporis diffusum of Fabry
- E75.250: Fabry's disease
- E75.510: Xanthoma, tendinous
- E75.520: Cerebrotendinous xanthomatosis
- E75.520: Xanthomatosis, cerebrotendinous
- E75.540: Lipid storage disease (NEC/NOS)
- E75.690: Lipid storage disease (NEC/NOS)
- E76.010: Mucopolysaccharidosis I H (Hurler)
- E76.010: Hurler syndrome (MPS I)
- E76.020: Gargoylism
- E76.040: Scheie syndrome
- E76.040: Mucopolysaccharidosis I S (Scheie)
- E76.120: Hunter syndrome (MPS II)
- E76.120: Mucopolysaccharidosis II (Hunter)
- E76.210: Morquio's syndrome
- E76.210: Mucopolysaccharidosis IV A & B (Morquio)
- E76.220: Sanfilippo syndrome
- E76.220: Mucopolysaccharidosis III A to D (Sanfilippo)
- E76.230: Mucopolysaccharidosis VI (Maroteaux-Lamy)
- E76.230: Maroteaux Lamy disease
- E76.280: Mucopolysaccharidosis, NEC
- E76.300: Mucopolysaccharidosis affecting the skin, NOS
- E78.210: Xanthoma, tubero-eruptive
- E78.220: Xanthoma, eruptive
- E78.230: Xanthoma, tuberous
- E78.240: Xanthoma disseminatum
- E78.250: Disseminated xanthosiderohistiocytosis
- E78.260: Xanthochromia striata palmaris
- E78.270: Xanthomatosis, NOS
- E78.280: Xanthoma, NOS
- E78.290: Diffuse normolipaemic plane xanthomatosis
- E78.500: Xanthomatosis due to hyperlipidaemia
- E78.660: Tangier disease
- E78.810: Urbach Wiethe disease
- E78.810: Lipoid proteinosis
- E78.810: Hyalinosis cutis et mucosae
- E78.810: Lipoid proteinosis
- E78.820: Hyalinosis, systemic
- E78.830: Multicentric reticulohistiocytosis
- E78.830: Multicentric reticulohistiocytosis
- E79.100: Lesch-Nyhan syndrome
- E80.010: Erythropoietic protoporphyria
- E80.010: Protoporphyria erythropoeitic
- E80.020: Gunther's disease
- E80.020: Erythropoietic porphyria, congenital
- E80.030: Porphyria, erythropoietic
- E80.040: Erythropoietic coproporphyria
- E80.100: Porphyria cutanea tarda
- E80.110: Porphyria cutanea tarda, sporadic
- E80.120: Porphyria cutanea tarda, familial
- E80.200: Porphyrin abnormality affecting the skin (NEC/NOS)
- E80.210: Porphyria, acute intermittent
- E80.210: Acute intermittent porphyria
- E80.220: Coproporphyria, hereditary
- E80.222: Hereditary coproporphyria
- E80.230: Variegate porphyria
- E80.232: Porphyria, Chester
- E80.232: Chester porphyria
- E80.240: Porphyria, hepatic
- E80.250: Pseudoporphyria
- E80.260: Toxic porphyria
- E80.282: Hepatoerythropoietic porphyria
- E80.290: Porphyria, NOS
- E83.010: Menkes' syndrome
- E83.010: Kinky hair disease
- E83.020: Wilson's disease
- E83.110: Haemochromatosis, skin changes due to
- E83.210: Acrodermatitis enteropathica
- E83.510: Calcinosis universalis
- E85.000: Amyloidosis, heredofamilial systemic affecting skin
- E85.100: Amyloidosis - familial amyloid polyneuropathy affecting skin
- E85.300: Amyloidosis secondary systemic
- E85.400: Amyloidosis, localized
- E85.800: Amyloidosis, NEC
- E85.900: Amyloidosis, NOS
- E88.010: Alpha 1 anti-trypsin deficiency
- E88.100: Lipodystrophy
- E88.110: Hollander Simons syndrome
- E88.120: Membranous lipodystrophy
- E88.120: Membranous lipodystrophy
- E88.130: Lipodystrophy, NEC
- E88.200: Multiple symmetrical lipomatosis
- E88.210: Adiposis dolorosa
- E88.210: Dercum's disease
- E88.280: Lipomatosis (NEC/NOS)
- E88.800: Lipomatosis, multiple symmetrical
- E88.820: Madelung's disease
- E88.820: Madelung's neck
F
[edit]- F06.010: Parasitophobia
- F45.800: Pruritus, psychogenic
- F63.300: Hair pulling
- F63.300: Trichotillomania
- F63.800: Trichotillomania
- F68.120: Münchhausen's syndrome
- F98.420: Trichophagia
- F98.810: Nail biting
- F98.810: Onychophagia
- F98.820: Onychotillomania
G
[edit]- G11.310: Ataxia telangiectasia
- G11.310: Louis Bar syndrome
- G51.200: Melkersson-Rosenthal syndrome
- G51.860: Hemiatrophy, facial
- G51.860: Romberg's syndrome
- G53.020: Neuralgia, post-herpetic
- G60.100: Heredopathia atactica polyneuritiformis
- G60.100: Refsum disease
- G71.110: Dystrophia myotonica
H
[edit]- H00.010: Hordeolum
- H00.100: Chalazion
- H01.000: Blepharitis
- H01.000: Blepharitis, NOS
- H01.110: Eyelid eczema
- H02.000: Entropion
- H02.010: Trichiasis (ingrowing eyelashes)
- H02.100: Ectropion
- H02.300: Blepharochalasis
- H02.690: Xanthelasma
- H02.710: Madarosis (loss of eyelashes)
- H04.200: Epiphora
- H10.100: Conjunctivitis, allergic
- H10.800: Conjunctivitis, nonallergic
- H10.900: Conjunctivitis
- H11.110: Pingueculae
- H11.210: Symblepharon acquired
- H16.110: Photokeratitis
- H30.810: Harada's disease
- H35.300: Angioid streaks
- H60.020: Furunculosis of external auditory canal
- H60.110: Streptococcal cellulitis of external ear
- H60.500: Acute otitis externa - eczematous
- H60.530: Otitis externa, acute
- H60.800: Otitis externa, chronic
- H60.900: Otitis externa
- H61.010: Chondrodermatitis nodularis of helix
- H61.020: Perichondritis of external ear
I
[edit]- I70.200: Atherosclerosis of arteries of extremit
- I70.230: Leg ulcer, ischaemic
- I70.231: Atherosclerotic ulcer
- I70.240: Atherosclerotic gangrene
- I70.240: Gangrene, ischaemic
- I70.240: Ischaemic foot ulcer
- I73.000: Raynaud's phenomenon
- I73.010: Raynaud's phenomenon, primary
- I73.020: Raynaud's phenomenon, secondary
- I73.030: Raynaud's disease
- I73.030: Raynaud's disease
- I73.040: Raynaud's gangrene
- I73.050: Digitus mortuus
- I73.100: Thromboangiitis obliterans
- I73.100: Thromboangiitis obliterans
- I73.810: Acrocyanosis
- I73.820: Erythromelalgia
- I73.830: Livedo reticularis
- I73.880: Lividities, symmetrical of soles
- I73.910: Microangiopathy of cutaneous vasculature, dermatosis due to (NEC)/(NOS)
- I73.990: Peripheral ischaemia
- I73.990: Ischaemia, peripheral
- I74.410: Embolism, arterial
- I77.800: Kohlmeier Degos syndrome
- I77.800: Malignant atrophic papulosis of Degos
- I77.800: Malignant atrophic papulosis of Degos
- I77.800: Papulosis, malignant atrophic
- I78.010: Telangiectasia, hereditary haemorrhagic
- I78.010: Angiomatosis Osler Weber Rendu
- I78.010: Osler Weber Rendu syndrome
- I78.110: Nevus araneus
- I78.110: Spider telangiectasis
- I78.110: Spider nevus
- I78.810: Telangiectasia, unilateral
- I78.820: Generalised essential telangiectasia
- I78.830: Telangiectasia
- I78.850: Capillaritis alba
- I78.850: Atrophie blanche en plaque
- I78.850: Hyalinising segmental vasculitis
- I80.000: Thrombophlebitis, superficial
- I80.220: Deep vein thrombosis in lower limb (NOS)
- I80.230: Phlegmasia cerulea dolens
- I80.810: Sclerosing periphlebitis of chest wall
- I80.810: Mondor's disease
- I80.900: Thrombophlebitis, NOS
- I80.910: Thrombophlebitis, NOS
- I80.920: Phlebothrombosis
- I82.100: Thrombophlebitis superficial migratory
- I82.820: Axillary vein thrombosis
- I82.830: Iliac vein thrombosis
- I82.830: Thrombosis, iliac vein
- I82.910: Venous thrombosis
- I83.000: Leg ulcer, venous
- I83.010: Ulcer, gravitational
- I83.010: Gravitational leg ulcer
- I83.010: Leg ulcer, varicose
- I83.030: Ulcer, stasis
- I83.030: Leg ulcer, post-phlebitic
- I83.100: Venous eczema
- I83.110: Eczema, gravitational
- I83.110: Eczema, stasis
- I83.110: Stasis eczema
- I83.110: Gravitational eczema
- I83.200: Ulcer, varicose with varicose eczema
- I83.200: Varicose ulcer with varicose eczema
- I83.910: Spider veins
- I83.920: Corona phlebectatica
- I83.990: Varicose veins
- I83.990: Varicosity, venous
- I83.990: Venous varix
- I84.500: External hemorrhoids, NOS
- I84.600: Anal skin tags
- I84.600: Skin tags of anus
- I86.000: Varicosities, sublingual
- I86.000: Sublingual varicosis
- I86.810: Palmar varices
- I86.820: Caput Medusae
- I86.820: Varicosities, abdominal due to portal hypertension
- I87.000: Post-thrombotic pre-ulcer stage
- I87.000: Post-phlebitic syndrome
- I87.000: Syndrome, postphlebitic
- I87.290: Acroangiodermatitis
- I89.000: Edema, lymphatic, NOS
- I89.000: Elephantiasis, NOS
- I89.000: Lymphoedema
- I89.010: Lymphedema, primary
- I89.020: Lymphedema, secondary
- I89.040: Lymphangiectasis
- I89.050: Elephantiasis
- I89.060: Elephantiasis nostras
- I89.100: Lymphangitis
- I89.840: Dermatopathic lymphadenopathy
- I89.840: Lymphadenopathy, dermatopathic
- I97.200: Lymphedema, postmastectomy
- I97.200: Post-mastectomy lymphedema
J
[edit]- J30.020: Rhinitis, vasomotor
- J30.210: Rhinitis, seasonal allergic
- J30.300: Rhinitis, perennial allergic
- J30.400: Allergy, respiratory NOS
- J31.010: Rhinitis, congestive non-allergic
- J33.900: Nasal polyposis
K
[edit]- K05.110: Marginal gingivitis
- K05.120: Gingivitis, chronic marginal
- K05.130: Gingivitis, desquamative
- K06.100: Gingival hyperplasia
- K06.800: Epulis giant cell
- K09.010: Dentigerous cyst
- K11.610: Oral mucous cyst
- K11.710: Xerostomia
- K11.810: Mikulicz syndrome
- K12.000: Aphthae, recurrent
- K12.000: Aphthous stomatitis, recurrent (RAS)
- K12.010: Minor aphthae (oral aphthosis)
- K12.010: Aphthous ulcers, herpetiform (oral aphthosis)
- K12.020: Periadenitis mucosa necrotica recurrens
- K12.030: Stomatitis aphthosa minor Mikulicz
- K12.030: Mikulicz ulcers
- K12.040: Sutton's aphthae (oral aphthosis)
- K12.040: Aphthous ulcers, major (oral aphthosis)
- K12.050: Bednar's aphthae
- K12.070: Aphthous ulcer of oral mucosa
- K12.090: Aphthous ulcers
- K12.100: Stomatitis
- K12.110: Stomatitis, acute
- K12.120: Ulcerative stomatitis
- K12.120: Stomatitis, ulcerative
- K12.140: Vesicular stomatitis
- K12.150: Pyostomatitis vegetans (inflammatory bowel disease)
- K13.000: Angular cheilitis
- K13.000: Angular cheilitis
- K13.000: Perlèche
- K13.002: Cheilodynie
- K13.010: Volkmann's cheilitis
- K13.020: Cheilitis simplex
- K13.040: Exfoliative cheilitis
- K13.052: Granulomatous cheilitis
- K13.060: Plasma cell cheilitis
- K13.062: Leukoplakia of lip
- K13.080: Lip fissure
- K13.090: Cheilitis
- K13.100: Cheek biting
- K13.110: Morsicatio buccarum
- K13.110: Frictional keratosis of oral mucosa
- K13.200: Leukoplakia
- K13.200: Oral leukoplakia
- K13.240: Leukoplakia of oral mucous membrane
- K13.250: Erythroplakia of oral mucous membrane
- K13.260: Leukokeratosis nicotina palati
- K13.300: Leukoplakia, oral hairy
- K13.300: Oral hairy leucoplakia
- K13.300: Oral hairy leukoplakia
- K13.300: Oral hairy leucoplakia
- K13.500: Oral submucous fibrosis
- K13.600: Oral verrucous hyperplasia
- K13.740: Gangrene infective of mouth
- K14.100: Geographical tongue
- K14.100: Geographical tongue
- K14.200: Median rhomboid glossitis
- K14.300: Hairy tongue
- K14.300: Tongue, hairy
- K14.310: Tongue, black hairy
- K14.310: Black hairy tongue
- K14.320: Papillitis, foliate
- K14.320: Foliate papillitis
- K14.410: Atrophic glossitis
- K14.500: Tongue, scrotal
- K14.600: Glossodynia
- K14.600: Burning tongue
- K14.810: Macroglossia
- K50.810: Crohn's disease of skin
- K59.400: Anal spasm
- K60.200: Fissure anal, NOS
- K60.200: Anal fissure, NOS
- K60.400: Rectal fistula
- K60.400: Fistula rectum to skin
- K61.300: Abscess, ischiorectal
- K61.300: Ischiorectal abscess
- K62.200: Anal prolapse
- K62.200: Prolapse of anal canal
- K90.000: Gluten sensitive enteropathy
- K90.000: Disease, celiac
- K90.000: Celiac disease
L
[edit]- L00.x00: Staphylococcal-Scalded-Skin-Syndrome (SSSS)
- L01.010: Staphylococcal impetigo
- L01.020: Streptococcal impetigo
- L01.030: Bulla repens
- L01.040: Impetigo follicularis
- L01.040: Impetigo follicularis
- L01.040: Impetigo, Bockhart's
- L01.090: Impetigo
- L01.090: Impetigo vulgaris
- L01.100: Impetiginisation (secondary)
- L02.900: Furuncle, Abscess, Carbuncle, NOS
- L02.910: Phagadenic abscess
- L02.920: Furuncle
- L02.930: Furunculosis
- L02.940: Carbuncle
- L02.950: Abscess
- L03.010: Panaritium
- L03.020: Paronychia
- L03.020: Acute paronychia, bacterial
- L03.050: Paronychia, acute bacterial
- L03.050: Perionychia, acute
- L03.050: Paronychia, acute bacterial
- L03.060: Paronychia, chronic
- L03.100: Cellulitis of other parts of the limbs
- L03.200: Cellulitis of face
- L03.300: Cellulitis of trunc
- L03.800: Cellulitis of other sites
- L03.900: Cellulitis, NOS
- L04.000: Lymphadenitis, acute of face, head or neck
- L04.100: Lymphadenitis, acute of trunc
- L04.200: Lymphadenitis, acute of upper limb
- L04.300: Lymphadenitis, acute of lower limb
- L04.900: Lymphadenitis acute
- L04.910: Abscess lymph node, NOS
- L04.920: Lymphangitis, acute
- L05.000: Abscess, pilonidal
- L05.010: Fistula, pilonidal with abscess
- L05.900: Cyst, pilonidal without abscess
- L05.910: Fistula, pilonidal without abscess
- L05.920: Sinus, pilonidal
- L05.930: Fistula, pilonidal
- L08.000: Pyoderma (bacterial)
- L08.010: Dermatitis, purulent
- L08.050: Chancriform pyoderma
- L08.050: Pyoderma, chancriform
- L08.100: Erythrasma
- L08.800: Infection of skin, NOS
- L08.802: Scar, infected
- L08.802: Infected scar
- L08.802: Cicatrix, infected
- L08.806: Intertrigo, streptococcal
- L08.810: Gram-negative infection of toe web
- L08.820: Erythema necrolyticum migrans
- L08.830: Ecthyma
- L08.840: Folliculitis, pustular
- L08.842: Folliculitis, gram-negative
- L08.850: Keratolysis, pitted
- L08.850: Keratoma plantare sulcatum
- L08.870: Fistula, NOS
- L08.880: Trichomycosis axillaris
- L08.900: Inflammation of skin, NOS
- L10.000: Pemphigus vulgaris
- L10.100: Pemphigus vegetans
- L10.120: Pyodermatitis vegetans
- L10.120: Pyodermite, végétante (Hallopeau)
- L10.120: Dermatitis vegetans
- L10.200: Pemphigus foliaceus
- L10.210: Cazenave's disease
- L10.300: Brazilian pemphigus
- L10.300: Wild fire pemphigus
- L10.300: Brazilian pemphigus
- L10.300: Pemphigus, Brazilian
- L10.400: Pemphigus erythematosus
- L10.400: Senear Usher syndrome
- L10.500: Pemphigus due to drug
- L10.500: Drug induced pemphigus
- L10.800: Pemphigus, NEC
- L10.800: Pemphigus, NEC
- L10.820: Paraneoplastic pemphigus
- L10.820: Pemphigus, paraneoplastic
- L10.820: Pemphigus paraneoplastica
- L10.900: Pemphigus
- L11.100: Dermatosis, transient acantholytic
- L11.100: Transient acantholytic dermatosis
- L11.100: Grover's disease
- L11.900: Acantholysis, NOS
- L12.000: Bullous pemphigoid
- L12.000: Pemphigoid, bullous
- L12.100: Mucous membrane pemphigoid
- L12.100: Cicatricial pemphigoid
- L12.110: Cicatricial pemphigoid, Brunsting-Perry type
- L12.120: Cicatrising conjunctivitis due to mucous membrane pemphigoid
- L12.200: Benign chronic bullous dermatosis of childhood
- L12.210: Juvenile pemphigoid
- L12.300: Epidermolysis acquisata
- L12.300: Acquired epidermolysis bullosa
- L12.310: Epidermolysis bullosa acquisita, drug-induced
- L12.310: Epidermolysis acquisata due to drug
- L12.800: Pemphigoid, NEC
- L12.900: Pemphigoid, NOS
- L13.000: Dermatitis herpetiformis
- L13.000: Duhring's disease
- L13.100: Subcorneal pustular dermatosis
- L13.100: Sneddon Wilkinson disease
- L13.800: Immunobullous disorder, unclassifiable
- L13.810: Linear IgA disease of childhood
- L13.820: Linear IgA disease of adulthood
- L13.850: Culicosis bullosa
- L13.900: Bullous dermatitis, NOS
- L20.000: Besnier's prurigo
- L20.000: Atopic dermatitis, prurigo
- L20.800: Atopic eczema, NEC
- L20.802: Atopic dermatitis, discoid pattern
- L20.804: Atopic dermatitis, inverse pattern
- L20.806: Atopic dermatitis, follicular
- L20.810: Atopic dermatitis, flexural
- L20.810: Flexural eczema
- L20.816: Eczema, infantile
- L20.816: Atopic dermatitis, infantile
- L20.828: Hand eczema, atopic
- L20.840: Atopic dermatitis, impetiginised
- L20.850: Erythrodermic atopic eczema
- L20.900: Atopic dermatitis
- L21.000: Seborrhoeic dermatitis of scalp
- L21.020: Seborrhoeic dermatitis of scalp
- L21.030: Pityriasis capitis
- L21.040: Milk crust seborrheic
- L21.100: Seborrhoeic dermatitis, infantile
- L21.110: Seborrhoeic dermatitis, infantile
- L21.120: Leiner syndrome
- L21.120: Erythroderma desquamativum
- L21.840: Seborrhoeic dermatitis, erythrodermic
- L21.900: Seborrhoeic dermatitis
- L21.900: Seborrhoeic dermatitis
- L22.x00: Napkin dermatitis
- L22.x00: Diaper rash
- L22.x10: Napkin psoriasis
- L22.x10: Napkin psoriasis
- L23.000: Allergic contact eczema due to metal
- L23.000: Allergy to metal
- L23.010: Allergic contact dermatitis - nickel
- L23.020: Allergic contact dermatitis - chromate
- L23.100: Allergic contact dermatitis - plastic, glue or resin system
- L23.200: Allergic contact dermatitis - cosmetic or toiletry
- L23.300: Allergic contact dermatitis - drug in contact with skin
- L23.300: Allergic contact dermatitis due to drugs
- L23.400: Allergic contact dermatitis due to dye
- L23.500: Allergic contact eczema due to other chemical products
- L23.510: Rubber dermatitis, NOS
- L23.510: Allergic contact eczema due to rubber
- L23.510: Allergic contact dermatitis - rubber chemical
- L23.520: Allergic contact dermatitis - insecticide
- L23.520: Allergic contact dermatitis - agrochemical
- L23.530: Allergic contact dermatitis - cement
- L23.540: Allergic contact dermatitis - plastic
- L23.700: Allergic contact dermatitis - plant
- L23.800: Allergic contact dermatitis - agent not elsewhere classified
- L23.810: Allergic contact dermatitis - airborne
- L23.810: Airborne contact dermatitis
- L24.000: Irritant contact dermatitis - detergents & wet work
- L24.100: Irritant Contact Dermatitis due to Oils and Greases
- L24.200: Irritant Contact Dermatitis due to Solvents
- L24.520: Irritant contact dermatitis - cement
- L24.700: Irritant contact dermatitis - contact with plant
- L24.800: Irritant Contact Dermatitis due to Specified Cause, NEC
- L24.910: Cumulative irritant contact dermatitis
- L24.920: Irritant contact dermatitis due to cumulative insult
- L24.930: Contact eczema, acute irritant, NOS
- L24.940: Chronic irritant contact eczema, NOS
- L25.900: Contact dermatitis, NOS
- L25.910: Occupational contact dermatitis, NOS
- L25.910: Occupational dermatitis
- L26.x00: Exfoliative dermatitis
- L26.x10: Pityriasis rubra Hebra
- L27.000: Generalised drug eruption
- L27.010: Erythema multiforme due to drug
- L27.030: Lichenoid drug eruption
- L27.050: Erythroderma due to drug
- L27.110: Fixed drug eruption
- L27.150: Bromoderma
- L28.000: Lichen simplex
- L28.100: Prurigo, nodular
- L28.210: Prurigo, nodular
- L28.210: Prurigo Hebra
- L28.210: Hebra's prurigo
- L28.220: Strophulus infantum
- L28.222: Urticaria papulosa
- L28.222: Prurigo, subacute
- L28.224: Prurigo, chronic
- L28.226: Prurigo pigmentosa
- L28.290: Prurigo
- L29.000: Pruritus ani
- L29.100: Pruritus scroti
- L29.200: Pruritus vulvae
- L29.300: Anogenital pruritus, NOS
- L29.830: Pruritus, aquagenic
- L29.830: Aquagenic pruritus
- L29.840: Pruritus, senile
- L29.850: Pruritus due to drug
- L29.850: Pruritus due to drug
- L29.860: Pruritus in diabetes mellitus
- L29.870: Uraemic pruritus
- L29.880: Pruritus due to liver disease
- L29.890: Generalised pruritus of unknown aetiology
- L29.900: Pruritus
- L30.000: Discoid eczema
- L30.000: Nummular dermatitis
- L30.100: Pompholyx
- L30.110: Cheiropompholyx
- L30.130: Cheiropodopompholyx
- L30.140: Podopompholyx
- L30.170: Juvenile plantar dermatosis
- L30.180: Dyshidrotic eczema
- L30.181: Vesicular eczema of hands and feet, chronic
- L30.190: Dyshidrosis
- L30.200: Autosensitisation dermatitis
- L30.205: Ide eruption
- L30.210: Mycide
- L30.220: Candidid
- L30.240: Id eruption due to eczema
- L30.300: Dermatitis, eczematoid
- L30.310: Infective eczema
- L30.310: Eczema, infective
- L30.400: Eczema, intertriginous
- L30.490: Intertrigo
- L30.500: Pityriasis alba faciei
- L30.590: Pityriasis alba
- L30.800: Dermatitis, NEC
- L30.802: Etat craquelé
- L30.806: Papuloerythroderma Ofuji
- L30.808: Pityriasis simplex
- L30.822: Eczema infantum
- L30.834: Hyperkeratotic palmar eczema
- L30.836: Psoriasiform palmar eczema
- L30.842: Lick eczema
- L30.852: Nipple eczema
- L30.862: Scrotal eczema
- L30.864: Anal eczema
- L30.864: Perianal eczema
- L30.910: Hand eczema
- L40.000: Psoriasis vulgaris
- L40.020: Psoriasis, Type 1 (early onset)
- L40.030: Psoriasis, Type 2 (late onset)
- L40.050: Psoriasis, nummular
- L40.100: Von Zumbusch's disease
- L40.100: Pustular psoriasis, generalised
- L40.110: Acute generalised pustular psoriasis
- L40.110: Psoriasis, acute generalised pustular
- L40.120: Impetigo herpetiformis
- L40.200: Acropustulosis
- L40.300: Psoriasis, chronic palmoplantar pustular
- L40.311: Palmoplantar pustulosis
- L40.380: Pustular bacterid
- L40.380: Pustular bacterid Andrews
- L40.400: Psoriasis, guttate
- L40.500: Psoriatic arthritis
- L40.510: Psoriasis, arthropathic
- L40.820: Circinate and annular pustular psoriasis
- L40.830: Flexural psoriasis
- L40.840: Psoriasis, intertriginous
- L40.850: Erythrodermic psoriasis
- L40.860: Nail psoriasis
- L41.000: Mucha Habermann disease
- L41.000: Pityriasis lichenoides acuta
- L41.000: Pityriasis lichenoides et varioliformis acuta
- L41.100: Pityriasis lichenoides chronica
- L41.200: Lymphomatoid papulosis
- L41.300: Parapsoriasis, small plaque
- L41.400: Parapsoriasis, large-plaque
- L41.800: Parapsoriasis, NEC
- L41.900: Parapsoriasis, NOS
- L42.x00: Pityriasis rosea
- L42.x00: Gibert's disease
- L43.000: Lichen planus, hypertrophic oral
- L43.100: Lichen planus, bullous
- L43.200: Lichenoid reaction due to drug
- L43.300: Lichen planus, subacute
- L43.310: Lichen planus tropicus
- L43.804: Lichen planus of nail
- L43.808: Lichen planus annularis
- L43.808: Lichen planus, annular
- L43.810: Lichen planus, oral
- L43.812: Lichen planus, linear
- L43.814: Lichen planus, atrophic
- L43.816: Lichen planus, verrucous
- L43.818: Lichen planus, generalised
- L43.820: Lichen planus, follicular
- L43.900: Lichen planus
- L44.000: Devergie's disease
- L44.000: Pityriasis rubra pilaris
- L44.010: Pityriasis rubra pilaris, adult forms
- L44.020: Pityriasis rubra pilaris, juvenile forms
- L44.030: Pityriasis rubra pilaris, juvenile - circumscribed (type IV)
- L44.100: Lichen nitidus
- L44.200: Lichen striatus
- L44.300: Lichen ruber moniliformis
- L44.400: Gianotti-Crosti syndrome
- L44.870: Tinea amiantacea
- L44.870: Pityriasis amiantacea
- L44.870: Pityriasis amiantacea
- L45.x00: Papulosquamous disorders in diseases classified elsewhere
- L50.000: Urticaria, allergic
- L50.000: Allergic urticaria
- L50.010: Urticaria due to food
- L50.020: Urticaria due to drug
- L50.100: Urticaria, nonallergic
- L50.100: Urticaria, idiopathic
- L50.110: Acute idiopathic urticaria
- L50.110: Urticaria acute idiopathic
- L50.120: Urticaria, chronic idiopathic
- L50.200: Urticaria, thermal
- L50.210: Urticaria, cold
- L50.220: Urticaria, familial cold
- L50.230: Heat Urticaria
- L50.230: Urticaria due to local heat
- L50.300: Factitious urticaria
- L50.300: Urticaria, factitial
- L50.310: Dermographic urticaria
- L50.310: Autographism
- L50.410: Urticaria, delayed pressure
- L50.500: Urticaria, cholinergic
- L50.510: Urticaria, cholinergic
- L50.600: Contact urticaria
- L50.830: Urticaria, aquagenic
- L50.900: Urticaria
- L51.100: Erythema multiforme, bullous
- L51.110: Erythema multiforme - severe mucosal form
- L51.120: Stevens–Johnson syndrome
- L51.130: Fuch's syndrome
- L51.140: Ectodermosis erosiva pluriorificialis
- L51.200: Toxic epidermal necrolysis
- L51.200: Lyell's disease, drug-induced
- L51.800: Erythema multiforme due to specified cause, NEC
- L51.810: Erythema multiforme due to herpes simplex infection
- L52.x00: Erythema nodosum
- L53.000: Toxic erythema
- L53.100: Erythema annulare centrifugum
- L53.200: Erythema marginatum
- L53.300: Erythema chronic figurate
- L53.320: Erythema perstans
- L53.330: Erythema gyratum repens
- L53.840: Palmar erythema
- L53.910: Erythema, NOS
- L55.050: Sunburn
- L55.050: Erythema, solar
- L56.000: Phototoxic drug reaction
- L56.100: Photo-allergic drug reaction
- L56.200: Phototoxic contact dermatitis
- L56.210: Photodermatitis due to plant
- L56.220: Phytophotodermatitis
- L56.230: Berloque dermatitis
- L56.240: Phototoxic eczema
- L56.240: Phototoxic dermatitis
- L56.300: Solar urticaria
- L56.400: Polymorphous light eruption
- L56.410: Prurigo estivalis
- L56.800: Dermatosis, acute due to UV
- L56.810: Folliculitis, actinic
- L56.850: Photo-onycholysis
- L56.860: Hydroa vacciniforme
- L57.000: Actinic keratosis
- L57.000: Solar keratosis
- L57.300: Poikiloderma of Civatte
- L57.400: Elastosis senilis
- L57.500: O'Brien's granuloma
- L57.500: Granuloma actinic
- L57.820: Favre Racouchot syndrome
- L57.862: Farmer's skin
- L57.862: Sailor's skin
- L57.870: Persistent light reaction
- L57.886: Colloid milium, acquired
- L57.890: Elastosis, solar
- L57.890: Actinic elastosis
- L57.900: Chronic solar damage to skin, NOS
- L58.000: Radiodermatitis, acute
- L58.100: Radiodermatitis, chronic
- L58.110: Radiation-induced dermatosis (NEC/NOS)
- L58.900: Radiodermatitis, NOS
- L59.000: Erythema ab igne
- L60.000: Ingrowing nail, NOS
- L60.010: Fingernail ingrowing
- L60.020: Ingrowing toenail
- L60.100: Onycholysis
- L60.110: Lamellar onycholysis
- L60.200: Onychogryphosis
- L60.300: Nail dystrophy
- L60.320: Nail dystrophy
- L60.340: Trachyonychia
- L60.350: Onychorrhexis
- L60.360: Onychodystrophy acquired
- L60.370: Twenty nail dystrophy
- L60.370: Twenty nail dystrophy
- L60.380: Dystrophia unguis mediana canaliformis
- L60.390: Nail dystrophy, NEC
- L60.400: Beau's lines
- L60.500: Yellow nail syndrome
- L60.804: Subungual hyperkeratosis
- L60.814: Anonychia, acquired
- L60.816: Nail artefact, NOS
- L60.818: Nail damage caused by chemical agents
- L60.818: Nail damage caused by chemicals
- L60.820: Leukopathia unguium due to drug
- L60.820: Leuconychia, drug-induced
- L60.822: Leuconychia, punctate
- L60.844: Trumpet nail deformity
- L60.860: Nail dystrophy due to trauma
- L60.862: Nail damage due to drug
- L60.864: Nail discolouration, exogeneous
- L60.872: Hematoma, subungual
- L60.872: Subungual haematoma
- L60.874: Splinter hemorrhage
- L60.876: Nail discolouration, endogeneous
- L60.878: Pterygium of nail
- L60.900: Nail disorder, NOS
- L62.800: Nail dystrophy due diseases classified elsewhere
- L62.810: Racket nails
- L62.830: Half-and-half nail
- L62.840: Lichen planus of nail
- L63.000: Alopecia totalis
- L63.100: Alopecia universalis
- L63.200: Alopecia areata, ophiasic
- L63.810: Alopecia areata, diffuse
- L63.900: Alopecia areata
- L64.000: Drug induced androgenic alopecia
- L64.810: Androgenetic alopecia due to androgen excess
- L64.820: Male pattern alopecia
- L64.820: Male pattern baldness
- L64.830: Alopecia, androgenic - female pattern
- L64.900: Alopecia androgenic, NOS
- L65.000: Telogen effluvium
- L65.100: Effluvium, anagen
- L65.200: Mucinosis, follicular
- L65.200: Follicular mucinosis
- L65.820: Alopecia, diffuse
- L65.830: Alopecia, diffuse due to drug
- L65.834: Alopecia due to malnutrition
- L65.836: Alopecia, diffuse postinfective
- L65.840: Alopecia diffuse, toxic
- L65.842: Alopecia, nonscarring traumatic
- L65.852: Alopecia, traction
- L65.852: Traction alopecia
- L65.854: Alopecia due to pressure
- L65.870: Loose anagen hair syndrome
- L65.900: Alopecia, nonscarring, NOS
- L65.910: Hair loss, NOS
- L66.000: Pseudopelade
- L66.100: Lichen planopilaris
- L66.120: Graham-Little syndrome
- L66.200: Folliculitis decalvans
- L66.300: Folliculitis abscedens et suffodiens
- L66.410: Ulerythema reticulata
- L66.800: Cicatricial alopecia, NEC
- L66.810: Alopecia parvimaculata
- L66.820: Alopecia, cicatricial due to trauma/injury
- L66.900: Cicatricial alopecia, NOS
- L67.000: Trichorrhexis nodosa
- L67.100: Variations in hair colour
- L67.110: Poliosis circumscripta, acquired
- L67.120: Canities
- L67.130: Premature greying
- L67.140: Heterochromia
- L67.150: Poliosis
- L67.800: Hair changes, NEC
- L67.810: Pili trianguli et canaliculi
- L67.812: Pili pseudoanulati
- L67.814: Pili bifurcati
- L67.820: Hair shaft disorder, NEC
- L67.830: Trichorrhexis invaginata
- L67.834: Trichoschisis
- L67.838: Trichoclasis
- L67.840: Trichomalacia
- L67.842: Trichonodosis
- L67.844: Fragile hair
- L67.860: Hair dystrophy, NEC
- L67.870: Hair colour change, NEC
- L67.900: Abnormal hair shaft, NOS
- L67.910: Hair shaft damage - exogeneous
- L67.920: Abnormal hair, NOS
- L68.000: Hirsutism
- L68.010: Hirsutism, endocrine
- L68.020: Hirsutism due to drug
- L68.030: Hirsutism, idiopathic
- L68.030: Hirsutism, idiopathic
- L68.100: Hypertrichosis lanuginosa, acquired
- L68.200: Hypertrichosis localised, NOS
- L68.800: Hypertrichosis, specified, NEC
- L68.830: Hypertrichosis due to drug
- L68.860: Hypertrichosis, idiopathic
- L68.900: Hypertrichosis
- L70.000: Acne vulgaris
- L70.010: Acne, comedonal
- L70.020: Acne, papulopustular
- L70.030: Acne, cystic
- L70.030: Acne indurata
- L70.100: Acne conglobata
- L70.300: Acne, tropical
- L70.400: Acne, infantile
- L70.812: Acne fulminans
- L70.814: Acne due to drug
- L70.816: Corticosteroid-induced acne
- L70.824: Iododerma
- L70.826: Bromoderma
- L70.828: Chloracne
- L70.830: Oil acne
- L70.830: Acne, oil
- L70.832: Acne, tar
- L70.834: Acne cosmetica
- L70.838: Acne, occupational
- L71.000: Perioral dermatitis
- L71.100: Rhinophyma
- L71.810: Rosacea, telangiectatic
- L71.820: Rosacea, pustular
- L71.850: Lupoid rosacea of Lewandowsky
- L71.900: Rosacea
- L72.000: Epidermoid cyst
- L72.100: Trichilemmal cyst
- L72.120: Scrotal cyst
- L72.200: Steatocystoma multiplex
- L72.200: Steatocystoma multiplex
- L72.820: Vellus hair cyst
- L72.830: Milium
- L73.100: Pseudofolliculitis barbae
- L73.200: Hidradenitis suppurativa
- L73.910: Folliculitis, NOS
- L74.000: Miliaria rubra
- L74.100: Miliaria crystallina
- L74.200: Miliaria profunda
- L74.420: Hypohidrosis
- L74.830: Granulosis rubra nasi
- L74.840: Ross syndrome
- L75.000: Bromhidrosis
- L75.100: Chromhidrosis
- L75.210: Fox-Fordyce disease
- L80.x00: Vitiligo
- L81.000: Hypermelanosis, post-inflammatory
- L81.100: Melasma
- L81.200: Ephelis
- L81.300: Café-au-lait macule
- L81.402: Lentiginosis, unilateral
- L81.404: Lentiginosis, eruptive
- L81.406: Lentiginosis, generalised
- L81.408: Hypermelanosis, periorbital
- L81.420: Lentigo simplex
- L81.438: Acromelanosis
- L81.448: Hypermelanosis
- L81.460: Laugier-Hunziker syndrome
- L81.540: Hypomelanosis, idiopathic guttate
- L81.750: Dermatite Gougerot-Blum
- L81.810: Tattoo, iron salt
- L81.820: Tattoo
- L81.824: Pigmentation due to carotenaemia
- L81.832: Pigmentation due to ingested/injected substance
- L81.854: Argyria
- L81.856: Chrysiasis
- L82.x20: Leser-Trélat syndrome
- L83.x00: Acanthosis nigricans
- L83.x10: Acanthosis nigricans, malignant
- L83.x20: Acanthosis nigricans, benign
- L83.x40: Confluent and reticulate papillomatosis of Gougerot & Carteaud
- L83.x40: Confluent and reticulate papillomatosis of Gougerot & Carteaud
- L83.x40: Confluent and reticulate papillomatosis of Gougerot & Carteaud
- L84.x00: Callosity
- L84.x00: Callosity
- L85.000: Ichthyosis, acquired
- L85.010: Pityriasis rotunda
- L85.020: Ichthyosiform reaction to drug
- L85.110: Keratoderma climactericum
- L85.140: Keratoderma, acquired
- L85.150: Bazex syndrome (acrokeratosis paraneoplastica)
- L85.150: Bazex syndrome (acrokeratosis paraneoplastica)
- L85.850: Acrokeratoelastoidosis of Costa
- L85.910: Hyperkeratosis, unspecified
- L87.000: Kyrle's disease
- L87.100: Reactive perforating collagenosis
- L87.200: Elastosis perforans serpiginosa
- L88.x00: Pyoderma gangrenosum
- L89.x00: Decubitus gangrene
- L89.x00: Decubitus gangrene
- L90.300: Atrophoderma of Pasini-Pierini
- L90.400: Acrodermatitis chronica atrophicans
- L90.510: Scar
- L90.510: Scar
- L90.520: Atrophic scarring
- L90.812: Cutaneous atrophy due to topical corticosteroid
- L90.814: Cutaneous atrophy due to corticosteroids
- L90.820: Atrophoderma, follicular
- L90.870: Lipoatrophy NOS
- L90.872: Lawrence Seip syndrome
- L90.872: Lipoatrophia totalis
- L90.876: Lipoatrophia semicircularis
- L90.900: Atrophy, cutaneous
- L90.910: Anetoderma
- L91.000: Keloid
- L91.030: Scar, hypertrophic
- L91.910: Pachyderma (NOS)
- L92.000: Granuloma annulare
- L92.020: Granuloma annulare, perforating
- L92.030: Granuloma annulare, generalised
- L92.040: Granuloma annulare, subcutaneous
- L92.100: Necrobiosis lipoidica
- L92.110: Necrobiosis lipoidica, non-diabetic
- L92.120: Granulomatosis disciformis chronica et progressiva
- L92.120: Miescher's granuloma
- L92.200: Granuloma faciale
- L92.300: Foreign body granuloma
- L92.300: Granuloma, foreign body
- L92.311: Suture materials in skin, reaction to
- L92.320: Sinus, barber's hair
- L92.320: Barber's hair sinus
- L92.800: Granuloma of skin, NEC
- L92.810: Oleoma
- L92.820: Oleogranuloma
- L92.830: Granuloma, infantile gluteal
- L92.840: Granuloma multiforme
- L92.850: Lipogranuloma, idiopathic sclerosing
- L92.850: Lipogranuloma, sclerosing
- L92.872: Oil granuloma
- L92.872: Paraffinoma
- L92.874: Silica granuloma
- L92.880: Granuloma, NEC
- L92.900: Granuloma of skin or subcutaneous tissue, NOS
- L93.000: Discoid lupus erythematosus
- L93.010: Lupus erythematosus
- L93.010: Lupus, non-tuberculous
- L93.020: Lupus erythematosus, chronic discoid
- L93.020: Discoid lupus erythematosus
- L93.100: Subacute cutaneous lupus erythematosus
- L93.200: Lupus erythematosus, cutaneous, NEC
- L93.210: Lupus erythematosus profundus
- L93.230: Lupus erythematodes tumidus
- L93.240: Lupus erythematodes verrucosus
- L93.260: Chilblain lupus erythematosus
- L93.270: Lupus panniculitis
- L94.000: Morphea, NOS
- L94.000: Morphoea
- L94.000: Circumscribed scleroderma
- L94.020: Guttate morphoea
- L94.020: Localised morphea
- L94.030: Morphoea, generalised
- L94.100: Scleroderma linear
- L94.100: Morphoea, linear
- L94.100: Morphoea en coup de sabre
- L94.120: Frontoparietal morphoea
- L94.120: En coup de sabre
- L94.200: Calcinosis cutis
- L94.210: Calcinosis dystrophica
- L94.220: Calculus, cutaneous
- L94.230: Calcinosis, acral
- L94.300: Sclerodactyly
- L94.400: Gottron's papules
- L94.500: Poikiloderma, prereticulotic
- L94.500: Prereticulotic poikiloderma
- L94.500: Poikiloderma vasculare atrophicans
- L94.600: Ainhum
- L94.610: Constricting band of extremity
- L94.620: Pseudo-ainhum
- L94.810: Pseudoscleroderma
- L94.820: Skleroedema adultorum Buschke
- L94.822: Skleroedema diabeticorum
- L94.830: Elastosis, cutaneous NEC
- L94.900: Connective tissue disease affecting skin (NEC/NOS)
- L95.000: Vasculitis, livedoid
- L95.000: Livedoid vasculitis
- L95.000: Livedoid vasculitis
- L95.020: Livedo reticularis with summer ulceration
- L95.100: Erythema elevatum diutinum
- L95.800: Capillaritis, NOS
- L95.810: Vasculitis, urticarial
- L95.820: Livedo racemosa
- L95.850: Nodular vasculitis
- L95.850: Vasculitis, nodular
- L95.850: Nodular vasculitis
- L95.900: Vasculitis, cutaneous
- L97.x00: Ulcer leg, NOS
- L97.x00: Leg ulcer, NOS
- L97.x00: Leg ulcer
- L98.000: Pyogenic granuloma
- L98.000: Granuloma pyogenicum
- L98.000: Pyogenic granuloma
- L98.010: Angioma, eruptive
- L98.100: Simulated dermatitis
- L98.100: Factitial dermatitis
- L98.100: Dermatitis artefacta
- L98.100: Self-inflicted skin disease (NEC/NOS)
- L98.100: Dermatitis, factitial
- L98.110: Factitious lymphoedema
- L98.120: Artefact, cutaneous
- L98.130: Excoriation(s), neurotic
- L98.130: Neurotic excoriation(s)
- L98.130: Neurotic excoriations
- L98.140: Purpura, psychogenic
- L98.200: Dermatosis, acute febrile neutrophilic
- L98.200: Sweet's syndrome
- L98.200: Acute febrile neutrophilic dermatosis
- L98.200: Sweet's disease
- L98.300: Eosinophilic cellulitis
- L98.300: Wells' syndrome
- L98.400: Ulcer, skin, NOS
- L98.400: Ulcer, chronic
- L98.420: Foot ulcer, neuropathic
- L98.420: Ulcer, neurotrophic
- L98.420: Neurotrophic ulcer
- L98.440: Tropical ulcer
- L98.440: Sore, tropical
- L98.440: Tropical ulcer
- L98.450: Ulcer, traumatic
- L98.490: Skin ulcer
- L98.500: Mucinosis, cutaneous (NEC/NOS)
- L98.500: Mucinosis, cutaneous NOS
- L98.520: Mucinosis, focal cutaneous
- L98.530: Lichen myxedematosus
- L98.540: REM syndrome
- L98.550: Plaque-like Mucinosis
- L98.560: Selfhealing juvenile cutaneous mucinosis
- L98.560: Mucinosis, self-healing juvenile cutaneous
- L98.580: Arndt Gottron syndrome
- L98.580: Scleromyxoedema
- L98.810: Pseudolymphoma of skin
- L98.812: Angiolymphoid hyperplasia with eosinophilia
- L98.820: Kimura´s disease
- L98.830: Lymphocytoma cutis
- L98.840: Lymphocytic infiltration
- L98.840: Benign lymphocytic infiltration of Jessner-Kanof
- L98.860: Erythema arciforme et palpabile migrans
- L98.880: Oid-Oid Disease
- L98.880: Sulzberger Garbe syndrome
- L98.880: Exudative discoid and lichenoid dermatitis
- L98.884: Ascher´s syndrome
- L98.910: Skin disease, NOS
- L98.910: Dermatosis, NOS
M
[edit]- M02.390: Balanitis, circinate (Reiter's disease)
- M02.390: Fiessinger Leroy syndrome
- M02.390: Vulvovaginitis, circinate (Reiter's disease)
- M02.390: Reiter's disease involving skin
- M05.290: Vasculitis, rheumatoid
- M05.290: Rheumatoid arteritis
- M06.390: Rheumatoid nodules
- M08.290: Still's disease juvenile
- M08.290: Still's disease, juvenile
- M10.091: Gouty tophus
- M30.000: Polyarteritis nodosa
- M30.000: Kussmall Meier disease
- M30.000: Polyarteritis nodosa
- M30.000: Periarteritis nodosa
- M30.020: Cutaneous polyarteritis nodosa
- M30.020: Polyarteritis nodosa, cutaneous
- M30.110: Churg Strauss granuloma
- M30.110: Allergic granulomatous angiitis
- M30.120: Granulomatosis, allergic
- M30.120: Allergic granulomatosis
- M30.300: Kawasaki disease
- M30.300: Kawasaki disease
- M30.300: Mucocutaneous lymphnode syndrome
- M30.810: Polyangiitis overlap syndrome
- M30.820: Sneddon's syndrome
- M30.820: Livedo reticularis with nodules
- M31.000: Hypersensitivity angiitis
- M31.010: Goodpasture syndrome
- M31.100: Thrombotic microangiopathy
- M31.110: Thrombotic thrombocytopenic purpura
- M31.110: Thrombocytopenic purpura, thrombotic
- M31.110: Purpura, thrombotic thrombocytopenic
- M31.300: Wegener's granulomatosis
- M31.310: Midline granuloma
- M31.400: Takayasu arteritis
- M31.400: Takayasu's arteritis
- M31.600: Giant cell arteritis, NOS
- M31.600: Giant cell arteritis
- M31.600: Arteritis, giant cell
- M31.610: Arteritis, temporal
- M31.610: Arteritis, giant cell
- M31.610: Horton's syndrome
- M31.610: Arteritis, temporal
- M31.800: Angiitis, necrotising NEC
- M31.810: Vasculitis, urticrial hypocomplementemic
- M32.000: Drug-induced lupus syndrome
- M32.010: Lupus erythematosus(LE)-like syndrome due to drug
- M32.900: Systemic lupus erythematosus
- M33.000: Dermatomyositis, juvenile
- M33.000: Juvenile dermatomyositis
- M33.100: Dermatomyositis, NEC
- M33.200: Polymyositis
- M33.900: Dermatopolymyositis, NOS
- M33.910: Dermatomyositis
- M34.000: Progressive systemic sclerosis
- M34.020: Systemic sclerosis, diffuse cutaneous type
- M34.100: CREST syndrome
- M34.210: Scleroderma occupational
- M34.830: Scleroderma (systemic), limited cutaneous type
- M34.860: Acrosclerosis
- M34.870: Thibierge Weissenbach syndrome
- M35.000: Sjögren syndrome
- M35.010: Keratoconjunctivitis sicca
- M35.040: Sicca syndrome
- M35.100: Mixed connective tissue disease
- M35.100: Overlap syndrome (connective tissue disease)
- M35.100: Sharp syndrome (mixed connective tissue disease)
- M35.100: Sclerodermatomyositis
- M35.200: Behçet's disease
- M35.210: Mouth and genital ulcer-Inflamed cartilage-syndrome (MAGIC-Syndrom)
- M35.210: MAGIC-Syndrom
- M35.400: Shulman's syndrome
- M35.400: Eosinophilic fasciitis
- M35.500: Fibrosclerosis multiple
- M35.600: Weber Christian disease
- M35.600: Systemic nodular panniculitis
- M35.600: Relapsing febrile nodular panniculitis (Weber-Christian)
- M35.600: Nodular non-suppurative febrile panniculitis
- M35.610: Panniculitis, relapsing
- M35.650: panniculitis due to alpha 1 anti-trypsin deficiency
- M35.900: Autoimmune systemic disease, NOS
- M35.920: Systemic connective disease, NOS
- M35.930: Collagen vascular disease, NOS
- M36.000: Dermatomyositis associated with internal malignancy
- M36.000: Malignant disease with dermatomyositis
- M67.490: Ganglion
- M70.810: Digital myxoid cyst
- M71.200: Baker's cyst
- M72.000: Fibromatosis, palmar
- M72.000: Palmar fibromatosis
- M72.000: Dupuytren's contracture
- M72.100: Knuckle pads
- M72.200: Plantar fibromatosis
- M72.200: Ledderhose's disease
- M72.200: Plantar fibromatosis
- M72.210: Plantar fasciitis
- M72.390: Nodular fasciitis
- M72.591: Ischaemic fasciitis
- M72.891: Hyalinosis, infantile systemic
- M72.891: Fibromatosis, juvenile hyaline
- M72.892: Fibromatosis, juvenile hyaline
- M72.893: Myofibromatosis, aggressive systemic infantile
- M72.893: Fibromatosis congenital generalised
- M72.895: Infantile digital fibromatosis
- M72.895: Fibromatosis, infantile digital
- M79.390: Panniculitis, NOS
- M79.894: Fat necrosis, traumatic
- M79.896: Panniculitis, cold
- M79.896: Panniculitis, cold
- M89.490: Pachydermoperiostosis
- M95.100: Ear, cauliflower
- M95.100: Ear, cauliflower
N
[edit]- N48.102: Balanitis
- N48.160: Balanitis, infective
- N48.170: Balanitis, irritant
- N48.180: Zoon's balanitis
- N48.180: Balanitis, plasma cell
- N48.190: Balanoposthitis
- N48.300: Priapism
- N48.300: Painful erection
- N48.500: Penile ulcer
- N48.500: Ulcer of penis
- N48.600: Balanitis xerotica obliterans
- N48.610: Peyronie's disease
- N48.610: Plastic induration of penis
- N48.610: Fibromatosis, penile
- N48.820: Phlebitis, Mondor's of penis
- N48.820: Mondor's phlebitis of penis
- N48.830: Chordee, nonvenereal
- N49.810: Gangrene, Fournier's
- N62.x00: Gynaecomastia
- N64.000: Mammillary fistula
- N64.520: Nipple, retracted acquired
- N75.000: Bartholin's gland cyst
- N75.100: Bartholin's gland cyst
- N75.800: Bartholinitis
- N76.020: Vulvovaginitis, acute
- N76.110: Vulvovaginitis, chronic
- N76.210: Vulvitis, NOS
- N76.600: Vulvar ulcer, NOS
- N76.610: Lipschütz ulcer (vulval aphthosis)
- N80.610: Endometriosis, cutaneous
- N84.300: Vulvar polyp
- N90.300: Vulvar dysplasia, NOS
- N90.410: Kraurosis vulvae
O
[edit]- O22.000: Varicose veins of leg in pregnancy
- O22.100: Vulvar varices in pregnancy
- O22.200: Superficial thrombophlebitis in pregnan
- O22.300: Deep vein thrombosis in pregnancy
- O26.400: Herpes gestationis
- O26.400: Pemphigoid gestationis
- O99.740: PUPPP syndrome (pruritic urticarial papules and plaques of pregnancy)
P
[edit]- P00.810: Lupus erythematosus, neonatal
- P00.820: Lupus erythematosus, neonatal
- P35.200: Herpes simplex congenital
- P35.200: Herpes simplex, neonatal
- P80.000: Neonatal cold injury
- P83.000: Sclerema neonatorum
- P83.100: Toxic erythema neonatorum
- P83.100: Erythema neonatorum
- P83.800: Subcutaneous fat necrosis of newborn
- P83.820: Bronze baby syndrome
Q
[edit]- Q17.000: Auricle, accessory
- Q18.010: Fistula, branchial
- Q18.020: Cyst, branchial
- Q27.400: Phlebectasia, diffuse congenital
- Q36.900: Hare lip
- Q38.200: Macroglossia, congenital
- Q69.900: Polydactyly
- Q70.900: Syndactyly
- Q77.300: Chondrodysplasia punctata
- Q78.420: Haemangiomata with dyschondroplasia
- Q80.020: Ichthyosis, follicular
- Q80.100: Ichthyosis, X-linked recessive
- Q80.200: Ichthyosis, lamellar
- Q80.870: Netherton syndrome (ichthyosis linearis circumflexa)
- Q81.000: Epidermolysis bullosa simplex
- Q81.010: Epidermolysis bullosa simplex (Köbner)
- Q81.020: Epidermolysis bullosa simplex with mottled pigmentation (Gedde-Dahl)
- Q81.030: Epidermolysis bullosa simplex (Weber-Cockayne)
- Q81.030: Epidermolysis bullosa simplex (Weber-Cockayne)
- Q81.100: Epidermolysis bullosa, junctional - lethal (Herlitz)
- Q81.200: Epidermolysis bullosa, dystrophic
- Q81.210: Epidermolysis bullosa, dystrophic - dominant (Pasini variant)
- Q81.240: Epidermolysis bullosa, dystrophic - inverse
- Q81.260: Epidermolysis bullosa, dystrophic - generalised recessive (Hallopeau-Siemens)
- Q81.820: Epidermolysis bullosa simplex herpetiformis (Dowling-Meara)
- Q81.850: Epidermolysis bullosa, junctional
- Q82.100: Xeroderma pigmentosum
- Q82.120: De Sanctis-Cacchione syndrome
- Q82.230: Mastocytosis, cutaneous
- Q82.290: Urticaria - pigmentosa
- Q82.296: Telangiectasia macularis eruptiva perstans
- Q82.300: Incontinentia pigmenti of Bloch-Sulzberger
- Q82.300: Incontinentia pigmenti of Bloch-Sulzberger
- Q82.502: Inflammatory Linear Verrucous Epidermal Nevus (ILVEN)
- Q82.503: Naevus, epidermal
- Q82.504: Nevus, aplastic
- Q82.505: Naevus, eccrine
- Q82.507: Naevus, apocrine
- Q82.509: Nevus syringocystadenomatosus papilliferus
- Q82.510: Port-wine stain
- Q82.520: Telangiectatic naevus
- Q82.540: Naevus anemicus
- Q82.550: Naevus, woolly hair
- Q82.552: Nevus lipomatodes superficialis
- Q82.570: Naevus sebaceus of Jadassohn
- Q82.582: Becker´s naevus
- Q82.585: Nevus, acantholytic
- Q82.597: Nevus, elastic
- Q82.802: Naevoid basal cell carcinoma syndrome
- Q82.810: Pseudoxanthoma elasticum, hereditary
- Q82.816: Cutis laxa
- Q82.817: Ehlers-Danlos syndrome
- Q82.818: Poikiloderma, congenital/genetic (NEC/NOS)
- Q82.832: Keratoderma, progressive palmoplantar (Greither)
- Q82.832: Keratoderma, progressive palmoplantar (Greither)
- Q82.834: Mal de Meleda
- Q82.836: Palmoplantar keratoderma, hereditary
- Q82.844: Poikiloderma with incontinentia pigmenti (Degos-Touraine)
- Q82.852: Rothmund-Thomson syndrome
- Q82.855: Erythrokeratoderma
- Q82.857: Erythrokeratoderma en cocardes (Degos syndrome)
- Q82.858: Erythrokeratoderma, symmetrical progressive of Gottron
- Q82.859: Erythrokeratoderma variabilis (Mendes da Costa)
- Q82.859: Erythrokeratoderma variabilis (Mendes da Costa)
- Q82.868: Darier's disease
- Q82.872: Acrokeratosis verruciformis (Hopf)
- Q82.878: Ectodermal dysplasia (NEC/NOS)
- Q82.882: Ectodermal dysplasia, hypohidrotic
- Q83.300: Nipple, accessory
- Q83.900: Breast, developmental defect
- Q84.010: Atrichia congenita
- Q84.110: Pili annulati
- Q84.120: Pili torti
- Q84.130: Uncombable hair syndrome
- Q84.140: Monilethrix
- Q84.160: Brittle hair (trichothiodystrophy)
- Q84.169: Trichothiodystrophy
- Q84.210: Hypertrichosis lanuginosa, congenital
- Q84.220: Hypertrichosis lanuginosa, congenital
- Q84.230: Marie-Unna syndrome
- Q84.256: Nevus, hair follicle
- Q84.300: Anonychia
- Q84.510: Pachyonychia congenita
- Q84.520: Pachyonychia congenita type I (Jadasssohn-Lewandowsky)
- Q84.530: Pachyonychia congenita type II (Jackson-Lawler)
- Q84.540: Pachyonychia congenita type III (Schafer-Brunauer)
- Q84.610: Nail deformity, inherited (NEC/NOS)
- Q84.810: Aplasia cutis congenita
- Q85.000: Neurofibromatosis - multiple neurofibromas
- Q85.010: Neurofibromatosis 1
- Q85.020: Neurofibromatosis II
- Q85.030: Neurofibromatosis, segmental
- Q87.110: Cockayne syndrome
- Q87.114: Russell-Silver syndrome
- Q87.136: Sjögren-Larsson syndrome
- Q87.170: Cornelia de Lange syndrome
- Q87.210: Klippel-Trenaunay-Weber syndrome
- Q87.210: Klippel-Trenaunay-Weber syndrome
- Q87.230: Nail-patella syndrome
- Q87.400: Marfan syndrome
- Q87.410: Arachnodactyly
- Q90.900: Down syndrome
- Q96.900: Turner syndrome
- Q98.400: Klinefelter syndrome
- Q99.200: Poly X syndrome
R
[edit]- R20.850: Dysesthesia, oral
- R20.850: Burning mouth syndrome
- R23.200: Flushing
- R23.840: Erythrocyanosis
- R60.030: Oedema due to heart failure
- R60.040: Oedema due to hypoproteinaemia
- R61.000: Hyperhidrosis, localised
- R61.030: Hyperhidrosis, axillary
- R61.040: Hyperhidrosis, asymmetrical
- R61.050: Hyperhidrosis, gustatory
- R61.100: Hyperhidrosis, generalised