autosomaal recessieve hereditaire aandoening
hereditaire ontwikkelingsstoornis
malformatiesyndroom met betrokkenheid van meerdere systemen
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oculotrichoanaal syndroom (aandoening)
oculotrichoanaal syndroom
MOTA
Manitoba oculotrichoanaal syndroom
Manitoba oculotrichoanal syndrome
MOTA - Manitoba oculotrichoanal syndrome
Marles-Greenburg-Persaud syndrome
Marles syndrome
Id703539006
StatusPrimitive
Associated morphologymorfologische afwijking
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
SNOMED CT to Orphanet simple map2717
SNOMED CT to ICD-10 extended map
TargetQ87.8
RuleTRUE
AdviceALWAYS Q87.8
CorrelationSNOMED CT source code to target map code correlation not specified