familiaire gegeneraliseerde lentiginosis (aandoening)
familiaire gegeneraliseerde lentiginosis
Familial generalized lentiginosis
Familial multiple lentigines syndrome without systemic involvement
Familial lentigines profusa
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.
Associated morphologylentigo
Finding sitestructuur van huid
Pathological processproces van pathologische ontwikkeling
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TermOverige vormen van hyperpigmentatie door melanine
SNOMED CT to Orphanet simple map231040
SNOMED CT to ICD-10 extended map
AdviceALWAYS L81.4
CorrelationSNOMED CT source code to target map code correlation not specified