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

• SNOMED CT Concept\Clinical finding\...
• \Viscus structure finding\Abdominal organ finding\Liver finding\Disorder of liver\Crigler-Najjar syndrome, type I
• \Digestive system finding\Liver finding\Disorder of liver\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\Disorder of liver\Crigler-Najjar syndrome, type I
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Crigler-Najjar syndrome, type I
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Liver finding\Disorder of liver\Crigler-Najjar syndrome, type I
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of liver\Crigler-Najjar syndrome, type I
• \Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\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\Disorder of liver\Crigler-Najjar syndrome, type I
• \Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\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\Disorder of bilirubin metabolism\Hyperbilirubinemia\Crigler-Najjar syndrome\Crigler-Najjar syndrome, type I
• \Disease\Metabolic disease\Disorder of porphyrin metabolism\Disorder of bilirubin metabolism\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, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

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

Expanded Value Set

This concept is not in any reference sets

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