autosomaal dominante hereditaire aandoening	brachydactylie	congenitale hallux varus	hereditaire aandoening van bewegingsapparaat	hereditaire ontwikkelingsstoornis	polymalformatief syndroom met defect van extremiteit als voornaamst kenmerk	verstandelijke beperking
\|	\|	\|	\|	\|	\|	\|

syndroom van brachydactylie en preaxiale hallux varus (aandoening)
	syndroom van brachydactylie en preaxiale hallux varus
	Brachydactyly and preaxial hallux varus syndrome
	A rare congenital limb malformation characterized the association of hallux varus with short thumbs and first toes (involving the metacarpals, metatarsals, and distal phalanges; the proximal and middle phalanges are of normal length) and abduction of the affected digits. Intellectual deficit was observed in all reported individuals. There have been no further reports since 1994.

Id	732957009
Status	Primitive

Associated morphology	abnormaal korte groei
Finding site	gehele digitus van hand of voet
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	varusmisvorming
Finding site	structuur van gewricht van digitus I van voet
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Has interpretation	gestoord
Interprets	intellectueel vermogen

Has interpretation	gestoord
Interprets	Adaptation behavior

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q73.8
Term	Overige onderontwikkeling van niet gespecificeerde extremiteit(en)

Target	Q66.3
Term	Overige congenitale varusmisvormingen van voeten

SNOMED CT to Orphanet simple map

1278

SNOMED CT to ICD-10 extended map

Target	Q87.2
Rule	TRUE
Advice	ALWAYS Q87.2 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified