Autosomal dominant hereditary disorder
Hereditary hypermelanosis
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Familial progressive hyperpigmentation (disorder)
Familial progressive hyperpigmentation
Melanosis diffusa congenita
Melanosis universalis hereditaria
Universal melanosis
Patches of hyperpigmentation in the skin, which are present at birth or in early infancy and increase in size and number with age. A rare autosomal dominant disorder.
melanosis diffusa congenita
melanosis universalis hereditaria
familiaire progressieve hyperpigmentatie
Id715630006
StatusPrimitive
Associated morphologyMelanosis
Finding siteSkin structure
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetL81.4
RuleTRUE
AdviceALWAYS L81.4
CorrelationSNOMED CT source code to target map code correlation not specified