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718106009: Hyperinsulinism and hyperammonemia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3304054016 Hyperinsulinism and hyperammonemia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3304055015 Hyperinsulinism and hyperammonemia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3304056019 Hyperinsulinism and hyperammonaemia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5285668015 GLUD1 related hyperinsulinism and hyperammonaemia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5285669011 Glutamate dehydrogenase 1 related hyperinsulinism and hyperammonemia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5285670012 GLUD1 related hyperinsulinism and hyperammonemia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5285671011 Glutamate dehydrogenase 1 related hyperinsulinism and hyperammonaemia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401675013 A rare diffuse form of congenital hyperinsulinism characterized by an excessive/ uncontrolled insulin secretion (inappropriate for the level of glycemia), chronic hyperammonemia and recurrent episodes of hypoglycemia induced by fasting and protein rich meals. Epilepsy and cognitive deficit, which are unrelated to hypoglycemia but possibly related to the chronic hyperammonemia, may also occur. This disorder is usually responsive to diazoxide treatment. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401676014 A rare diffuse form of congenital hyperinsulinism characterised by an excessive/ uncontrolled insulin secretion (inappropriate for the level of glycaemia), chronic hyperammonaemia and recurrent episodes of hypoglycaemia induced by fasting and protein rich meals. Epilepsy and cognitive deficit, which are unrelated to hypoglycaemia but possibly related to the chronic hyperammonaemia, may also occur. This disorder is usually responsive to diazoxide treatment. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperinsulinism and hyperammonemia syndrome (disorder) Is a Hyperammonemia true Inferred relationship Some
Hyperinsulinism and hyperammonemia syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hyperinsulinism and hyperammonemia syndrome (disorder) Is a Hyperinsulinism true Inferred relationship Some
Hyperinsulinism and hyperammonemia syndrome (disorder) Is a Hereditary disorder of endocrine system (disorder) true Inferred relationship Some
Hyperinsulinism and hyperammonemia syndrome (disorder) Finding site Endocrine pancreatic structure false Inferred relationship Some
Hyperinsulinism and hyperammonemia syndrome (disorder) Is a Digestive system hereditary disorder (disorder) true Inferred relationship Some
Hyperinsulinism and hyperammonemia syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Hyperinsulinism and hyperammonemia syndrome (disorder) Finding site Endocrine pancreatic structure true Inferred relationship Some 1
Hyperinsulinism and hyperammonemia syndrome (disorder) Is a Congenital disease (disorder) false Inferred relationship Some
Hyperinsulinism and hyperammonemia syndrome (disorder) Is a Inborn error of metabolism true Inferred relationship Some
Hyperinsulinism and hyperammonemia syndrome (disorder) Is a Disorder of digestive system specific to fetus OR newborn true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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