Autosomal recessive hereditary disorder	Crigler-Najjar syndrome	Digestive system hereditary disorder	Disease of liver	Disorder of digestive system specific to fetus OR newborn
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Crigler-Najjar syndrome, type I (disorder)
	Crigler-Najjar syndrome, type I
	Crigler-Najjar syndrome type I Bilirubin glucuronosyltransferase deficiency Deficiency of glucuronosyltransferase Crigler-Najjar type 1 UDP glucuronyl transferase deficiency Glucuronyltransferase deficiency Bilirubin UDP glucuronyl transferase deficiency

Id	8933000
Status	Primitive

Finding site

Liver structure

Occurrence

SNOMED CT to Orphanet simple map

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	E80.5
Term	Syndroom van Crigler-Najjar

SNOMED CT to ICD-10 extended map

Target	E80.5
Rule	TRUE
Advice	ALWAYS E80.5
Correlation	SNOMED CT source code to target map code correlation not specified