FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

237939006: Non-ketotic hyperglycinemia (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
356613013 Disorder of glycine cleavage enzyme complex en Synonym Active Entire term case insensitive SNOMED CT core module
356614019 NKH - Non-ketotic hyperglycinaemia en Synonym Active Entire term case sensitive SNOMED CT core module
356615018 Non-ketotic hyperglycinaemia en Synonym Active Entire term case insensitive SNOMED CT core module
356616017 NKH - Non-ketotic hyperglycinemia en Synonym Active Entire term case sensitive SNOMED CT core module
356617014 Non-ketotic hyperglycinemia en Synonym Active Entire term case insensitive SNOMED CT core module
626744019 Non-ketotic hyperglycinemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3037061014 Non ketotic hyperglycinemia en Synonym Active Entire term case insensitive SNOMED CT core module
3037470016 Non ketotic hyperglycinaemia en Synonym Active Entire term case insensitive SNOMED CT core module

8 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Non-ketotic hyperglycinemia Is a Hyperglycinemia true Inferred relationship Existential restriction modifier
Non-ketotic hyperglycinemia Finding site Body system structure false Inferred relationship Existential restriction modifier
Non-ketotic hyperglycinemia Occurrence Congenital false Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Non-ketotic hyperglycinemia H protein deficiency Is a True Non-ketotic hyperglycinemia Inferred relationship Existential restriction modifier
Non-ketotic hyperglycinemia L protein deficiency Is a True Non-ketotic hyperglycinemia Inferred relationship Existential restriction modifier
Glycine dehydrogenase (decarboxylating) deficiency Is a True Non-ketotic hyperglycinemia Inferred relationship Existential restriction modifier
Aminomethyltransferase deficiency Is a True Non-ketotic hyperglycinemia Inferred relationship Existential restriction modifier
Childhood-onset spasticity with hyperglycinemia Is a True Non-ketotic hyperglycinemia Inferred relationship Existential restriction modifier
Infantile glycine encephalopathy Is a True Non-ketotic hyperglycinemia Inferred relationship Existential restriction modifier
Atypical glycine encephalopathy Is a True Non-ketotic hyperglycinemia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start