autosomaal recessieve hereditaire aandoening	congenitaal lang-QT-intervalsyndroom	congenitaal perceptief gehoorverlies	congenitale afwijking van hart	congenitale geleidingsstoornis	hereditair gehoorverlies	hereditaire ontwikkelingsstoornis
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Jervell-Lange-Nielsen-syndroom (aandoening)
	Jervell-Lange-Nielsen-syndroom
	audito-cardiaal syndroom syndroom van Jervell-Lange-Nielsen
	Jervell and Lange-Nielsen syndrome
	Cardio-auditory syndrome

Id	373905003
Status	Primitive

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

Interprets

Finding site	structuur van auditief systeem
Occurrence	congenitaal

DHD Diagnosis thesaurus reference set

SNOMED CT to Orphanet simple map

90647

SNOMED CT to ICD-10 extended map

Target	I45.8
Rule	TRUE
Advice	ALWAYS I45.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified