autosomaal dominante hereditaire aandoening	distale artrogrypose	hereditaire artrogrypose
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distale artrogrypose type 1 (aandoening)
	distale artrogrypose type 1
	DA1
	Digitotalar dysmorphism
	Distal arthrogryposis type 1
	An autosomal dominant congenital anomaly characterized by contractures of the distal regions of the hands and feet with no facial involvement or any additional anomalies. It is the most common type of distal arthrogryposis.

Id	715314008
Status	Primitive

Associated morphology	contractuur
Finding site	structuur van gewrichtsregio
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Has interpretation	verlaagd
Interprets	'range of motion' van gewricht

Associated morphology	contractuur
Finding site	structuur van gewricht van meerdere lichaamsregio's

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q68.8
Term	Overige gespecificeerde congenitale misvormingen van botspierstelsel

SNOMED CT to Orphanet simple map

1146

SNOMED CT to ICD-10 extended map

Target	Q68.8
Rule	TRUE
Advice	ALWAYS Q68.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified