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238063003: Loss of multiple peroxisomal functions (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
356845017 Loss of multiple peroxisomal functions en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626894014 Loss of multiple peroxisomal functions (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


6 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
chondrodysplasie ponctuée rhizomélique est un(e) (attribut) True Loss of multiple peroxisomal functions Inferred relationship Some
Zellweger's-like syndrome est un(e) (attribut) True Loss of multiple peroxisomal functions Inferred relationship Some
Pseudoinfantile Refsum's disease est un(e) (attribut) True Loss of multiple peroxisomal functions Inferred relationship Some

This concept is not in any reference sets

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