FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

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
790111000052116 förlust av multipla peroxisomala funktioner sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Loss of multiple peroxisomal functions Is a Disorder of peroxisomal function true Inferred relationship Some
Loss of multiple peroxisomal functions Occurrence Congenital true Inferred relationship Some 1
Loss of multiple peroxisomal functions Finding site Body system structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Zellweger's-like syndrome Is a True Loss of multiple peroxisomal functions Inferred relationship Some
Pseudoinfantile Refsum's disease Is a True Loss of multiple peroxisomal functions Inferred relationship Some
Rhizomelic chondrodysplasia punctata syndrome Is a True Loss of multiple peroxisomal functions Inferred relationship Some

This concept is not in any reference sets

Back to Start