autosomaal dominante hereditaire aandoening	congenitale afwijking van sternum	hereditaire aandoening van bewegingsapparaat	hereditaire ontwikkelingsstoornis	polymalformatief syndroom met defect van extremiteit als voornaamst kenmerk	syndactylie
\|	\|	\|	\|	\|	\|

acropectoraal syndroom (aandoening)
	acropectoraal syndroom
	syndroom van syndactylie, preaxiale polydactylie en misvorming van sternum ACRP-syndroom
	Acropectoral syndrome
	Syndactyly with preaxial polydactyly and sternal deformity syndrome Acro-pectoral syndrome
	Syndrome with characteristics of a combination of distal limb abnormalities (syndactyly of all fingers and toes, preaxial polydactyly in the feet and/or hands) and upper sternum malformations. It has been described in 22 patients from a six-generation Turkish family. It is transmitted as an autosomal dominant trait and the causative gene is located at 7q36.

Id	720412009
Status	Primitive

Associated morphology	morfologische afwijking
Finding site	botstructuur van sternum
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	Abnormally fused structure
Finding site	structuur van digitus van hand of voet
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q74.0
Term	Overige congenitale misvormingen van bovenste extremiteit(en), inclusief schoudergordel

SNOMED CT to Orphanet simple map

85203

SNOMED CT to ICD-10 extended map

Target	Q74.0
Rule	TRUE
Advice	ALWAYS Q74.0 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified