ILDS

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

 


ICD sorted by Disorder:
Poliosis - Post-kala-azar dermal leishmaniasis

ICD Code Disorder
L67.150:
Poliosis
L67.110:
Poliosis circumscripta, acquired
Q99.200:
Poly X syndrome
M30.810:
Polyangiitis overlap syndrome
M30.000:
Polyarteritis nodosa
M30.000:
Polyarteritis nodosa
M30.020:
Polyarteritis nodosa, cutaneous
E28.200:
Polycystic ovary syndrome, cutaneous manifestations of
D45.x00:
Polycythaemia vera
Q69.900:
Polydactyly
L56.400:
Polymorphous light eruption
M33.200:
Polymyositis
L30.100:
Pompholyx
C44.L67:
Porocarcinoma, eccrine
E80.100:
Porphyria cutanea tarda
E80.120:
Porphyria cutanea tarda, familial
E80.110:
Porphyria cutanea tarda, sporadic
E80.210:
Porphyria, acute intermittent
E80.232:
Porphyria, Chester
E80.030:
Porphyria, erythropoietic
E80.240:
Porphyria, hepatic
E80.290:
Porphyria, NOS
E80.200:
Porphyrin abnormality affecting the skin (NEC/NOS)
Q82.510:
Port-wine stain
B55.010:
Post-kala-azar dermal leishmaniasis
 

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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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