FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

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
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
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


8 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Non-ketotic hyperglycinaemia Is a Hyperglycinemia true Inferred relationship Some
Non-ketotic hyperglycinaemia Finding site Body system structure false Inferred relationship Some
Non-ketotic hyperglycinaemia Occurrence Congenital false Inferred relationship Some

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

Reference Sets

GB English

US English

Back to Start