autosomaal recessieve hereditaire aandoening	chronische ziekte van bewegingsapparaat	hereditaire aandoening van bewegingsapparaat	hereditaire ontwikkelingsstoornis	osteogenesis imperfecta
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Mesoderm development LRP chaperone gene related osteogenesis imperfecta (disorder)
	MESD gene related osteogenesis imperfecta
	Osteogenesis imperfecta type XX Mesoderm development LRP chaperone gene related osteogenesis imperfecta

Id	1402321007
Status	Primitive

Clinical course

Has interpretation	afwijkend
Interprets	ossificatie

Associated morphology	dysplasie
Finding site	botstructuur
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

SNOMED CT to ICD-10 extended map

Target	Q78.0
Rule	TRUE
Advice	ALWAYS Q78.0
Correlation	SNOMED CT source code to target map code correlation not specified