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238066006: Loss of single peroxisomal function (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
356848015 Loss of single peroxisomal function en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626897019 Loss of single peroxisomal function (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


15 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Loss of single peroxisomal function localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Loss of single peroxisomal function survenue (attribut) congénital true Inferred relationship Some 1
Loss of single peroxisomal function est un(e) (attribut) Disorder of peroxisomal function true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Contiguous ABCD1 DXS1357E deletion syndrome (disorder) est un(e) (attribut) True Loss of single peroxisomal function Inferred relationship Some
Acyl-coenzyme A oxidase deficiency (disorder) est un(e) (attribut) True Loss of single peroxisomal function Inferred relationship Some
Adrenoleukodystrophy est un(e) (attribut) True Loss of single peroxisomal function Inferred relationship Some
Primary hyperoxaluria, type I est un(e) (attribut) True Loss of single peroxisomal function Inferred relationship Some
Acatalasemia est un(e) (attribut) True Loss of single peroxisomal function Inferred relationship Some
Peroxisomal thiolase deficiency est un(e) (attribut) True Loss of single peroxisomal function Inferred relationship Some
Bifunctional peroxisomal enzyme deficiency est un(e) (attribut) True Loss of single peroxisomal function Inferred relationship Some
Glutaryl-coenzyme A oxidase deficiency (disorder) est un(e) (attribut) True Loss of single peroxisomal function Inferred relationship Some
Dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia est un(e) (attribut) True Loss of single peroxisomal function Inferred relationship Some
Isolated dihydroxyacetone phosphate acyltransferase deficiency est un(e) (attribut) True Loss of single peroxisomal function Inferred relationship Some
Isolated alkyldihydroxyacetone phosphate synthase deficiency est un(e) (attribut) True Loss of single peroxisomal function Inferred relationship Some
Leukoencephalopathy, dystonia, motor neuropathy syndrome est un(e) (attribut) True Loss of single peroxisomal function Inferred relationship Some

This concept is not in any reference sets

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