congenitale afwijking van benig skelet	dysplasie met verhoogde botdichtheid
\|	\|

familiaire pachydermoperiostose (aandoening)
	familiaire pachydermoperiostose
	Pachydermoperiostosis - familial
	Familial hypertrophic osteoarthropathy

Id	254133005
Status	Primitive

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

Has interpretation	boven referentiebereik
Interprets	botdensitometrie

SNOMED CT to ICD-10 extended map

Target	M89.49
Rule	TRUE
Advice	ALWAYS M89.49 \| MAPPED FOLLOWING WHO GUIDANCE
Correlation	SNOMED CT source code to target map code correlation not specified