autosomaal dominante hereditaire aandoening	congenitale hereditaire endotheeldystrofie
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congenitale hereditaire endotheeldystrofie type 1 (aandoening)
	congenitale hereditaire endotheeldystrofie type 1
	Congenital hereditary endothelial dystrophy type 1
	Congenital hereditary endothelial dystrophy autosomal dominant form CHED1 - congenital hereditary endothelial dystrophy type 1

Id	416633008
Status	Primitive

Associated morphology	dystrofie
Finding site	structuur van endotheel van cornea

Associated morphology	cellulaire en/of subcellulaire afwijking
Finding site	chromosomenpaar 20
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	H18.5
Term	Hereditaire corneadystrofieën

SNOMED CT to Orphanet simple map

98975

SNOMED CT to ICD-10 extended map

Target	H18.5
Rule	TRUE
Advice	ALWAYS H18.5
Correlation	SNOMED CT source code to target map code correlation not specified