arthrogryposis multiplex congenita	autosomaal recessieve hereditaire aandoening	hereditaire artrogrypose	polyartropathie bij andere aandoening
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neurogene arthrogryposis multiplex congenita (aandoening)
	neurogene arthrogryposis multiplex congenita
	Neurogenic arthrogryposis multiplex congenita
	A form of arthrogryposis multiplex congenital characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscular atrophy.

Id	715316005
Status	Primitive

Due to

denervatie-atrofie van spier

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

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

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q74.3
Term	Arthrogryposis multiplex congenita

SNOMED CT to Orphanet simple map

1143

SNOMED CT to ICD-10 extended map

Target	Q74.3
Rule	TRUE
Advice	ALWAYS Q74.3 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

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syndroom van artrogrypose, nierfunctiestoornis en cholestase