Disorder of skin pigmentation
Hereditary disorder of the integument
||
Genetic disorder of skin pigmentation (disorder)
Genetic disorder of skin pigmentation
genetische aandoening van huidpigmentatie
erfelijke ziekte van huidpigmentatie
Id724839001
StatusDefined
Associated morphologyPigment alteration
Finding siteSkin structure
ICD-10 complex map reference set
TargetL81.9
RuleTRUE
AdviceALWAYS L81.9
CorrelationSNOMED CT source code to target map code correlation not specified
|
Albinism with deafness syndrome
Carney complex
Deaf blind hypopigmentation syndrome Yemenite type
Deafness, vitiligo, achalasia syndrome
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome
Familial progressive hyper and hypopigmentation
Gastrocutaneous syndrome
Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome
Hereditary hypermelanosis10
Inherited cutaneous hyperpigmentation12
Legius syndrome
Neuroectodermal melanolysosomal disease
Neurofibromatosis type 6
Oculocerebral hypopigmentation syndrome of Preus type
Oculocutaneous albinism10
Osteoporosis and oculocutaneous hypopigmentation syndrome
Palmoplantar hyperkeratosis-hyperpigmentation syndrome of Cantu
Phylloid hypomelanosis
Piebald trait with neurologic defects syndrome
Piebaldism
Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome
Reticulate acropigmentation of Kitamura
Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome
Vici syndrome
Waardenburg's syndrome5
X-linked reticulate pigmentary disorder with systemic manifestation syndrome
Xeroderma pigmentosum11