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238060000: General loss 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
356842019 General loss of peroxisomal function en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626891018 General loss of peroxisomal function (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Alpha-methylacyl-CoA racemase deficiency disorder est un(e) (attribut) True General loss of peroxisomal function Inferred relationship Some
Neonatal adrenoleukodystrophy est un(e) (attribut) False General loss of peroxisomal function Inferred relationship Some
Infantile Refsum's disease est un(e) (attribut) False General loss of peroxisomal function Inferred relationship Some

This concept is not in any reference sets

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