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870287007: Pelizaeus Merzbacher like disease due to GJC2 mutation (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3968815010 Pelizaeus Merzbacher like disease due to GJC2 mutation (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3968816011 Pelizaeus Merzbacher like disease due to GJC2 mutation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
14512591000172119 maladie PML (Pelizaeus-Merzbacher-like) due à une mutation du gène GJC2 fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
14512601000172112 maladie Pelizaeus-Merzbacher-like due à une mutation du gène GJC2 fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
4786751000172118 Pelizaeus-Merzbacher-achtige ziekte door GJC2-mutatie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pelizaeus Merzbacher like disease due to GJC2 mutation (disorder) Is a Pelizaeus Merzbacher like disease (disorder) true Inferred relationship Some
Pelizaeus Merzbacher like disease due to GJC2 mutation (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Pelizaeus Merzbacher like disease due to GJC2 mutation (disorder) Finding site White matter structure of brain and spinal cord (body structure) true Inferred relationship Some 1
Pelizaeus Merzbacher like disease due to GJC2 mutation (disorder) Finding site Myelinated nerve fiber structure true Inferred relationship Some 2
Pelizaeus Merzbacher like disease due to GJC2 mutation (disorder) Associated morphology Myelin sheath alteration true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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