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familiaire gegeneraliseerde lentiginosis (aandoening)
familiaire gegeneraliseerde lentiginosis
Familial generalized lentiginosis
Familial lentigines profusa
Familial multiple lentigines syndrome without systemic involvement
A rare inherited skin hyperpigmentation disorder with characteristics of widespread lentigines without associated noncutaneous abnormalities. Patients present multiple brown to dark brown, non-elevated macula of 0.2 to 1 cm in diameter, spread over the entire body, sometimes including palms or soles, but never oral mucosa.
Id765195000
StatusPrimitive
Associated morphologylentigo
Finding sitestructuur van huid
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
referentieset met complexe 'mapping' naar ICD-10
TargetL81.4
RuleTRUE
AdviceALWAYS L81.4
CorrelationSNOMED CT source code to target map code correlation not specified