autosomaal recessieve hereditaire aandoening
hereditaire aandoening van bewegingsapparaat
hereditaire ontwikkelingsstoornis
osteogenesis imperfecta
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Wnt family member 1 gene related osteogenesis imperfecta (disorder)
WNT1 gene related osteogenesis imperfecta
Wnt family member 1 gene related osteogenesis imperfecta
Osteogenesis imperfecta type XV
Id1402320008
StatusPrimitive
Has interpretationafwijkend
Interpretsossificatie
Associated morphologydysplasie
Finding sitebotstructuur
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
SNOMED CT to ICD-10 extended map
TargetQ78.0
RuleTRUE
AdviceALWAYS Q78.0
CorrelationSNOMED CT source code to target map code correlation not specified