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870286003: Pelizaeus Merzbacher like disease due to AIMP1 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
3968813015 Pelizaeus Merzbacher like disease due to AIMP1 mutation (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3968814014 Pelizaeus Merzbacher like disease due to AIMP1 mutation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4722191000052111 Pelizaeus Merzbacher-liknande sjukdom orsakad av AIMP1-mutation sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pelizaeus Merzbacher like disease due to AIMP1 mutation (disorder) Is a Pelizaeus Merzbacher like disease (disorder) true Inferred relationship Some
Pelizaeus Merzbacher like disease due to AIMP1 mutation (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Pelizaeus Merzbacher like disease due to AIMP1 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 AIMP1 mutation (disorder) Finding site Myelinated nerve fiber structure true Inferred relationship Some 2
Pelizaeus Merzbacher like disease due to AIMP1 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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