hereditaire ontwikkelingsstoornis
malformatiesyndroom met betrokkenheid van meerdere systemen
X-gebonden hereditaire dominante aandoening
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oculofaciocardiodentaal syndroom (aandoening)
oculofaciocardiodentaal syndroom
syndromale microftalmie 2
OFCD-syndroom
syndroom met microftalmie, cataract, radiculomegalie en hartseptumdefect
microftalmie-cataract-radiculomegalie-hartseptumdefect-syndroom
MCOPS2
Oculofaciocardiodental syndrome
Microphthalmia, cataract, radiculomegaly and septal heart defect
Oculo-facio-cardio-dental syndrome
Microphthalmia syndromic 2
Id699300009
StatusPrimitive
Associated morphologymorfologische afwijking
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
SNOMED CT to Orphanet simple map
SNOMED CT to ICD-10 extended map
TargetQ87.8
RuleTRUE
AdviceALWAYS Q87.8
CorrelationSNOMED CT source code to target map code correlation not specified