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237939006: Non-ketotic hyperglycinemia (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
3037061014 Non ketotic hyperglycinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3037470016 Non ketotic hyperglycinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356613013 Disorder of glycine cleavage enzyme complex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356614019 NKH - Non-ketotic hyperglycinaemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
356615018 Non-ketotic hyperglycinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356616017 NKH - Non-ketotic hyperglycinemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
356617014 Non-ketotic hyperglycinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626744019 Non-ketotic hyperglycinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


8 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Non-ketotic hyperglycinaemia localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Non-ketotic hyperglycinaemia survenue (attribut) congénital false Inferred relationship Some
Non-ketotic hyperglycinaemia est un(e) (attribut) Hyperglycinemia true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Childhood-onset spasticity with hyperglycinemia (disorder) est un(e) (attribut) True Non-ketotic hyperglycinaemia Inferred relationship Some
Non-ketotic hyperglycinemia H protein deficiency est un(e) (attribut) True Non-ketotic hyperglycinaemia Inferred relationship Some
Non-ketotic hyperglycinaemia L protein deficiency est un(e) (attribut) True Non-ketotic hyperglycinaemia Inferred relationship Some
Infantile glycine encephalopathy (disorder) est un(e) (attribut) True Non-ketotic hyperglycinaemia Inferred relationship Some
Atypical glycine encephalopathy est un(e) (attribut) True Non-ketotic hyperglycinaemia Inferred relationship Some
Glycine dehydrogenase (decarboxylating) deficiency est un(e) (attribut) True Non-ketotic hyperglycinaemia Inferred relationship Some
Aminomethyltransferase deficiency est un(e) (attribut) True Non-ketotic hyperglycinaemia Inferred relationship Some

Reference Sets

Canada French language reference set (foundation metadata concept)

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