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771441005: Hyperbiliverdinemia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3706210014 Hyperbiliverdinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706211013 Hyperbiliverdinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706212018 Hyperbiliverdinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706208012 A rare genetic hepatic disease characterised by the presence of green colouration of the skin, urine, plasma and other body fluids (ascites, breastmilk) or parts (sclerae) due to increased serum levels of biliverdin in association with biliary obstruction and/or liver failure. Association with malnutrition, medication, and congenital biliary atresia has also been reported. Can be caused by heterozygous or homozygous mutation in the gene encoding bilirubin reductase-alpha (BLVRA) on chromosome 7p13. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3706209016 A rare genetic hepatic disease characterized by the presence of green coloration of the skin, urine, plasma and other body fluids (ascites, breastmilk) or parts (sclerae) due to increased serum levels of biliverdin in association with biliary obstruction and/or liver failure. Association with malnutrition, medication, and congenital biliary atresia has also been reported. Can be caused by heterozygous or homozygous mutation in the gene encoding bilirubin reductase-alpha (BLVRA) on chromosome 7p13. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3706210014 Hyperbiliverdinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706211013 Hyperbiliverdinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706212018 Hyperbiliverdinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706208012 A rare genetic hepatic disease characterised by the presence of green colouration of the skin, urine, plasma and other body fluids (ascites, breastmilk) or parts (sclerae) due to increased serum levels of biliverdin in association with biliary obstruction and/or liver failure. Association with malnutrition, medication, and congenital biliary atresia has also been reported. Can be caused by heterozygous or homozygous mutation in the gene encoding bilirubin reductase-alpha (BLVRA) on chromosome 7p13. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3706209016 A rare genetic hepatic disease characterized by the presence of green coloration of the skin, urine, plasma and other body fluids (ascites, breastmilk) or parts (sclerae) due to increased serum levels of biliverdin in association with biliary obstruction and/or liver failure. Association with malnutrition, medication, and congenital biliary atresia has also been reported. Can be caused by heterozygous or homozygous mutation in the gene encoding bilirubin reductase-alpha (BLVRA) on chromosome 7p13. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3452601001000112 Hyperbiliverdinämie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
887731000172119 hyperbiliverdinémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
890941000172112 jaunisse verte fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
887731000172119 hyperbiliverdinémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
890941000172112 jaunisse verte fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3452601001000112 Hyperbiliverdinämie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperbiliverdinaemia Interprets Pyrrole measurement true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperbiliverdinaemia Is a Biliverdin above reference range (finding) true Inferred relationship Existential restriction modifier (core metadata concept)
Hyperbiliverdinaemia Finding site Liver structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperbiliverdinaemia Is a Autosomal hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hyperbiliverdinaemia Is a Disease of liver true Inferred relationship Existential restriction modifier (core metadata concept)
Hyperbiliverdinaemia Has interpretation Above reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperbiliverdinaemia Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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