FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

64852002: Sarcosine dehydrogenase deficiency (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
107791015 Sarcosine dehydrogenase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
107792010 Sarcosinuria en Synonym Active Entire term case insensitive SNOMED CT core module
107793017 Sarcosinemia en Synonym Active Entire term case insensitive SNOMED CT core module
107794011 Hypersarcosinemia en Synonym Active Entire term case insensitive SNOMED CT core module
107795012 Deficiency of the sarcosine dehydrogenase complex en Synonym Active Entire term case insensitive SNOMED CT core module
107796013 Demethylation defect of N-methylglycine en Synonym Active Only initial character case insensitive SNOMED CT core module
499975015 Sarcosinaemia en Synonym Active Entire term case insensitive SNOMED CT core module
499976019 Hypersarcosinaemia en Synonym Active Entire term case insensitive SNOMED CT core module
804291015 Sarcosine dehydrogenase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sarcosine dehydrogenase deficiency Is a Enzymopathy true Inferred relationship Existential restriction modifier
Sarcosine dehydrogenase deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Sarcosine dehydrogenase deficiency Is a Disorder of glycine metabolism true Inferred relationship Existential restriction modifier
Sarcosine dehydrogenase deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Sarcosine dehydrogenase deficiency Finding site Body system structure false Inferred relationship Existential restriction modifier
Sarcosine dehydrogenase deficiency Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start