Congenital anomaly of skin
Disorder of skin pigmentation
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Congenital pigmentary skin anomalies (disorder)
Congenital pigmentary skin anomalies
Congenital pigmentary anomaly of skin
congenitale pigmentafwijkingen van huid
Id205564003
StatusDefined
Associated morphologyPigment alteration
Finding siteSkin structure
OccurrenceCongenital
Pathological processPathological developmental process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ82.8
RuleTRUE
AdviceALWAYS Q82.8
CorrelationSNOMED CT source code to target map code correlation not specified
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Birthmark3
Carney complex
Carney complex, trismus, pseudocamptodactyly syndrome
Congenital deficiency of pigment of skin10
Familial generalized lentiginosis
Familial progressive hyper and hypopigmentation
Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome
Inherited cutaneous hyperpigmentation12
McCune Albright syndrome
Neuroectodermal melanolysosomal disease
Pseudoleprechaunism syndrome Patterson type