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syndroom van gingivale fibromatose en hypertrichose (aandoening)
syndroom van gingivale fibromatose en hypertrichose
CGHT
Gingival fibromatosis and hypertrichosis syndrome
Hirsutism congenital gingival hyperplasia syndrome
A rare autosomal dominant disorder characterized by a generalized enlargement of the gingiva occurring at birth or during childhood that is associated with generalized hypertrichosis developing at birth, during the first years of life, or at puberty and predominantly affecting the face, upper limbs, and midback.
Id716008002
StatusPrimitive
Associated morphologyverandering in groei
Finding sitestructuur van pilus
Associated morphologyfibromatose
Finding sitestructuur van gingiva
DHD Diagnosethesaurus-referentieset
DHD Verrichtingenthesaurus-referentieset
referentieset met complexe 'mapping' naar ICD-10
TargetK06.1
RuleTRUE
AdviceALWAYS K06.1
CorrelationSNOMED CT source code to target map code correlation not specified
TargetL68.8
RuleTRUE
AdviceALWAYS L68.8
CorrelationSNOMED CT source code to target map code correlation not specified