autosomaal dominante hereditaire aandoening	congenitale afwijking van hart	hereditaire aandoening van cardiovasculair systeem	hereditaire ontwikkelingsstoornis	situs ambiguus
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syndroom van hartanomalie en heterotaxie (aandoening)
	syndroom van hartanomalie en heterotaxie
	Cardiac anomaly and heterotaxy syndrome
	This syndrome has characteristics of non-compaction of the ventricular myocardium, bradycardia, pulmonary valve stenosis and secundum atrial septal defect. Laterality sequence anomalies are also present. So far, the syndrome has been described in nine members from three generations of the same family. Transmission is autosomal dominant and linkage to chromosome 6p24.3-21.2 was reported.

Id	720605009
Status	Primitive

Associated morphology	morfologische afwijking
Finding site	structuur van hart
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	malpositie
Finding site	structuur van inwendig orgaan
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	Q28.8
Term	Overige gespecificeerde congenitale misvormingen van hart en vaatstelsel

SNOMED CT to Orphanet simple map

137628

SNOMED CT to ICD-10 extended map

Target	Q28.8
Rule	TRUE
Advice	ALWAYS Q28.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified