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238059005: Disorder of 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
356841014 Disorder of peroxisomal function en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626890017 Disorder of peroxisomal function (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


41 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Liver disease due to peroxisomal disease Due to True Disorder of peroxisomal function Inferred relationship Some 2
General loss of peroxisomal function est un(e) (attribut) True Disorder of peroxisomal function Inferred relationship Some
Loss of multiple peroxisomal functions est un(e) (attribut) True Disorder of peroxisomal function Inferred relationship Some
Loss of single peroxisomal function est un(e) (attribut) True Disorder of peroxisomal function Inferred relationship Some
Peroxisome biogenesis disorder est un(e) (attribut) True Disorder of peroxisomal function Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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