autosomaal dominante hereditaire aandoening	hereditaire ontwikkelingsstoornis	osteochondrodysplasiesyndroom
\|	\|	\|

spondylo-epimetafysaire dysplasie Strudwick-type (aandoening)
	spondylo-epimetafysaire dysplasie Strudwick-type
	SEMD Strudwick-type
	Spondyloepimetaphyseal dysplasia, Strudwick type
	Dappled metaphysis syndrome Strudwick syndrome SEMD - spondyloepimetaphyseal dysplasia, Strudwick type

Id	702350003
Status	Primitive

Associated morphology	morfologische afwijking
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

SNOMED CT to Orphanet simple map

SNOMED CT to ICD-10 extended map

Target	Q77.7
Rule	TRUE
Advice	ALWAYS Q77.7
Correlation	SNOMED CT source code to target map code correlation not specified