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238067002: Peroxisomal thiolase deficiency (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
356849011 Peroxisomal thiolase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356850011 Pseudo-Zellweger syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
356851010 3-Ketoacyl-CoA thiolase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
626899016 Peroxisomal thiolase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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