autosomaal dominante hereditaire aandoening	distale artrogrypose	dwerggroei	hereditaire artrogrypose	palatoschisis
\|	\|	\|	\|	\|

distale artrogrypose type 3 (aandoening)
	distale artrogrypose type 3
	Distal arthrogryposis type 3
	Distal arthrogryposis type IIA Gordon syndrome Camptodactyly, cleft palate, clubfoot syndrome
	Distal arthrogryposis type 3 is an autosomal dominant non-progressive myopathy with contractures of the hands, ankle and feet along with cleft palate and short stature.

Id	897570002
Status	Primitive

Associated morphology	fusiedefect door stoornis in ontwikkeling
Finding site	structuur van palatum
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

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

Has interpretation	onder referentiebereik
Interprets	lengtemeting van lichaam

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

SNOMED CT to Orphanet simple map

376

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