autosomaal recessieve hereditaire aandoening
hereditaire aandoening van bewegingsapparaat
hereditaire ontwikkelingsstoornis
osteogenesis imperfecta
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FKBP prolyl isomerase 10 gene related osteogenesis imperfecta (disorder)
FKBP10 gene related osteogenesis imperfecta
Osteogenesis imperfecta type XI
FKBP prolyl isomerase 10 gene related osteogenesis imperfecta
Id1402322000
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