8933000: Crigler-Najjar syndrome, type I (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Viscus structure finding\Abdominal organ finding\Liver finding\Liver disease\Crigler-Najjar syndrome, type I
• \Digestive system finding\Liver finding\Liver disease\Crigler-Najjar syndrome, type I
• \Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Crigler-Najjar syndrome, type I
• \Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Liver disease\Crigler-Najjar syndrome, type I
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Crigler-Najjar syndrome, type I
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Liver finding\Liver disease\Crigler-Najjar syndrome, type I
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Liver disease\Crigler-Najjar syndrome, type I
• \Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Crigler-Najjar syndrome, type I
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of bilirubin metabolism\Crigler-Najjar syndrome\Crigler-Najjar syndrome, type I
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Crigler-Najjar syndrome, type I
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Crigler-Najjar syndrome, type I
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Crigler-Najjar syndrome\Crigler-Najjar syndrome, type I
• \Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Crigler-Najjar syndrome, type I
• \Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Crigler-Najjar syndrome, type I
• \Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Liver disease\Crigler-Najjar syndrome, type I
• \Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Crigler-Najjar syndrome, type I
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of bilirubin metabolism\Crigler-Najjar syndrome\Crigler-Najjar syndrome, type I
• \Disease\Metabolic disease\Enzymopathy\Crigler-Najjar syndrome\Crigler-Najjar syndrome, type I
• \Disease\Metabolic disease\Disorder of porphyrin metabolism\Bilirubin metabolism disorder\Hyperbilirubinaemia\Crigler-Najjar syndrome\Crigler-Najjar syndrome, type I
• \Disease\Metabolic disease\Disorder of porphyrin metabolism\Bilirubin metabolism disorder\Inherited disorder of bilirubin metabolism\Crigler-Najjar syndrome\Crigler-Najjar syndrome, type I
• \Disease\Congenital disease\Inborn error of metabolism\Inherited disorder of bilirubin metabolism\Crigler-Najjar syndrome\Crigler-Najjar syndrome, type I

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
15747010	Crigler-Najjar syndrome, type I	en	Synonym	Active	Case sensitive	SNOMED CT core
15748017	Deficiency of glucuronosyltransferase	en	Synonym	Active	Case insensitive	SNOMED CT core
15749013	Glucuronyltransferase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
15750013	UDP glucuronyl transferase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
508458016	Crigler-Najjar type 1	en	Synonym	Active	Case sensitive	SNOMED CT core
508459012	Bilirubin UDP glucuronyl transferase deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
508462010	Bilirubin glucuronosyltransferase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
508463017	Crigler-Najjar syndrome type I	en	Synonym	Active	Case sensitive	SNOMED CT core
832201013	Crigler-Najjar syndrome, type I (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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