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syndroom van hypertrichose en acromegaloïde aangezichtskenmerken (aandoening)
syndroom van hypertrichose en acromegaloïde aangezichtskenmerken
syndroom van hypertrichose en acromegaloïde gelaatskenmerken
syndroom van hypertrichose en acromegaloïd aangezicht
HAFF-syndroom
Hypertrichosis and acromegaloid facial appearance syndrome
Hypertrichosis acromegaloid facial features syndrome
Hypertrichosis coarse face syndrome
A very rare multiple congenital abnormality syndrome manifesting from birth with progressive hypertrichosis congenita terminalis (thick scalp hair extending onto the forehead with generalized increased body hair) associated with a typical acromegaloid facial appearance (thick eyebrows, prominent supraorbital ridges, broad nasal bridge, anteverted nares, long and large philtrum, and prominent mouth with full lips) appearing during childhood.
Id721837000
StatusPrimitive
Associated morphologyverandering in groei
Finding sitestructuur van pilus
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
referentieset met complexe 'mapping' naar ICD-10
TargetQ87.0
RuleTRUE
AdviceALWAYS Q87.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified