autosomaal recessieve hereditaire aandoening	congenitale microcefalie	gedilateerde cardiomyopathie	hereditaire aandoening van cardiovasculair systeem	hereditaire ontwikkelingsstoornis	malformatiesyndroom met betrokkenheid van meerdere systemen	verstandelijke beperking
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syndroom van microcefalie en cardiomyopathie (aandoening)
	syndroom van microcefalie en cardiomyopathie
	syndroom van Winship-Viljoen-Leary
	Microcephalus cardiomyopathy syndrome
	Microcephaly cardiomyopathy syndrome Winship Viljoen Leary syndrome
	Syndrome with characteristics of severe intellectual deficit, microcephaly and dilated cardiomyopathy. Hand and foot anomalies have also been reported. The syndrome has been described in three individuals. Transmission is autosomal recessive.

Id	719380003
Status	Primitive

Associated morphology	afwijkend klein
Finding site	structuur van hoofd
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Has interpretation	onder referentiebereik
Interprets	hoofdomtrek bij geboorte

Associated morphology	dilatatie
Finding site	structuur van myocardium

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	Q87.8
Term	Overige gespecificeerde congenitale gestoorde-ontwikkelingssyndromen, niet elders geclassificeerd

SNOMED CT to Orphanet simple map

2515

SNOMED CT to ICD-10 extended map

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified