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43123004: Hypermethioninemia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
71937014 Hypermethioninemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
493531016 Hypermethioninaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
780099018 Hypermethioninemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
936531000052115 hypermetioninemi sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypermethioninemia Is a Disorder of sulphur-bearing amino acid metabolism true Inferred relationship Some
Hypermethioninemia Occurrence Congenital false Inferred relationship Some
Hypermethioninemia Finding site Body system structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Neonatal hypermethioninemia Is a True Hypermethioninemia Inferred relationship Some
Hepatic methionine adenosyltransferase deficiency Is a True Hypermethioninemia Inferred relationship Some
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (disorder) Is a True Hypermethioninemia Inferred relationship Some
Hypermethioninemia due to deficiency of glycine N-methyltransferase Is a True Hypermethioninemia Inferred relationship Some
Hypermethioninemia encephalopathy due to deficiency of adenosine kinase (disorder) Is a True Hypermethioninemia Inferred relationship Some

This concept is not in any reference sets

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