ILDS

Application to Dermatology of International Classification of Disease (ICD-10)

 


ICD sorted by Disorder:
Basal cell carcinoma, recurrent - Blastomycosis, cutaneous

ICD Code Disorder
C44.L38:
Basal cell carcinoma, recurrent
C44.L21:
Basalioma
L85.150:
Bazex syndrome (acrokeratosis paraneoplastica)
L85.150:
Bazex syndrome (acrokeratosis paraneoplastica)
A18.482:
Bazin's disease
T88.120:
BCG ulcer
B35.040:
Beard ringworm
L60.400:
Beau's lines
Q82.582:
Becker´s naevus
C49.M30:
Bednar tumour
K12.050:
Bednar's aphthae
M35.200:
Behçet's disease
A65.x00:
Bejel
D76.320:
Benign cephalic histiocytosis
L12.200:
Benign chronic bullous dermatosis of childhood
L98.840:
Benign lymphocytic infiltration of Jessner-Kanof
A28.110:
benign Lymphoreticulosis
L56.230:
Berloque dermatitis
D86.920:
Besnier Boeck Schaumann disease
L20.000:
Besnier's prurigo
B65.900:
Bilharziasis, NOS
D48.520:
BK-Mole syndrome, hereditary
K14.310:
Black hairy tongue
D69.810:
Black heel
B40.300:
Blastomycosis, cutaneous
 

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Disorder
Code & Disorder

Abnormal hair shaft, NOSAcne, infantileAcute generalised pustular psoriasisAllergic contact dermatitis - cosmetic or toiletryAlopecia due to pressureAnal fissure, NOSAngiolupoidApocrine adenocarcinomaAtopic dermatitis, prurigoBalanitisBasal cell carcinoma, recurrentBlepharitisBurkitt's lymphoma in HIV diseaseCandida balanitisCapillaritis, NOSChediak Higashi syndromeChronic hyperplastic candidiasisConfluent and reticulate papillomatosis of Gougerot & CarteaudCryptococcosis of skinCysticercosis of skinDermatitis, NECDiabetic microangiopathy, dermatoses due toDrug-induced lupus syndromeEctodermosis erosiva pluriorificialisEndometriosis, cutaneousEpithelioma calcificans MalherbeErythema multiforme, bullousErythropoietic porphyria, congenitalFibrofolliculomas, multipleFistula, pilonidal with abscessFragile hairGeographical tongueGonococcal infection, otherGranuloma of skin or subcutaneous tissue, NOSHaemangiopericytomaHead liceHerpes simplex, primary ocularHistiocytosis, familial sea-blueHurler syndrome (MPS I)Hyperthyroidism, NOSImmunobullous disorder, unclassifiableIododermaKaposi's sarcoma, NOSKlinefelter syndromeLeg ulcer, NOSLeprosy, borderline lepromatousLeukoplakia of lipLichen scrofulosorumLipomatosis (NEC/NOS)Lupus erythematosus(LE)-like syndrome due to drugLymphangioma circumscriptumMadelung's diseaseMalignant melanoma, mucosalMetageriaMorphoeaMucormycosis, rhinocerebralMyiasisNaevus, woolly hairNecrobiotic xanthogranulomaNevus, acantholyticOculocutaneous albinism - tyrosinase-negative (type 1)Oral hairy leucoplakiaPachyonychia congenita type I (Jadasssohn-Lewandowsky)Papulosquamous disorders in diseases classified elsewherePemphigoid, bullousPerlèchePiedra albaPityriasis rubra HebraPoliosisPost-mastectomy lymphedemaPrurigo, subacutePsoriasis, arthropathicPustular bacterid AndrewsReactive perforating collagenosisRingworm of groinSarcoidosis, nodularSclerosing periphlebitis of chest wallSheehan's syndromeSore, tropicalStomatitis aphthosa minor MikuliczSurgical wound, dehiscenceSyphilitic chancre, genitalTattoo, iron saltTinea barbaeToxic shock syndromeTrichonodosisTuberculosis, wartyUlerythema reticulataVagabond's diseaseVerrucous dermatitisWarts, handXanthoma, tendinous
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