771441005: Hyperbiliverdinemia (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Measurement finding\...

\Finding of substance level\Increased biliverdin\Hyperbiliverdinaemia

\Measurement finding outside reference range\Measurement finding above reference range\Increased biliverdin\Hyperbiliverdinaemia

\Viscus structure finding\Abdominal organ finding\Liver finding\Liver disease\Hyperbiliverdinaemia

\Digestive system finding\Liver finding\Liver disease\Hyperbiliverdinaemia
\Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Hyperbiliverdinaemia
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Liver disease\Hyperbiliverdinaemia

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Hyperbiliverdinaemia
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Liver finding\Liver disease\Hyperbiliverdinaemia
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Liver disease\Hyperbiliverdinaemia
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Hyperbiliverdinaemia

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Hyperbiliverdinaemia
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hyperbiliverdinaemia
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Hyperbiliverdinaemia
\Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Hyperbiliverdinaemia
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Liver disease\Hyperbiliverdinaemia
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Hyperbiliverdinaemia

Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3706210014 Hyperbiliverdinaemia en Synonym Active Case insensitive SNOMED CT core

3706211013 Hyperbiliverdinemia (disorder) en Fully specified name Active Case insensitive SNOMED CT core

3706212018 Hyperbiliverdinemia en Synonym Active Case insensitive 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 Case sensitive 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 Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hyperbiliverdinaemia	Interprets	Pyrrole measurement	true	Inferred relationship	Some	1
Hyperbiliverdinaemia	Is a	Increased biliverdin	true	Inferred relationship	Some
Hyperbiliverdinaemia	Finding site	Liver structure	true	Inferred relationship	Some	2
Hyperbiliverdinaemia	Is a	Autosomal hereditary disorder	true	Inferred relationship	Some
Hyperbiliverdinaemia	Is a	Liver disease	true	Inferred relationship	Some
Hyperbiliverdinaemia	Has interpretation	Above reference range	true	Inferred relationship	Some	1
Hyperbiliverdinaemia	Is a	Digestive system hereditary disorder	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3706210014	Hyperbiliverdinaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
3706211013	Hyperbiliverdinemia (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3706212018	Hyperbiliverdinemia	en	Synonym	Active	Case insensitive	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	Case sensitive	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	Case sensitive	SNOMED CT core