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870286003: Pelizaeus Merzbacher like disease due to AIMP1 mutation (disorder)


Status: current, Primitive. 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 Case sensitive SNOMED CT core
3968814014 Pelizaeus Merzbacher like disease due to AIMP1 mutation en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pelizaeus Merzbacher like disease due to AIMP1 mutation Is a Pelizaeus Merzbacher like disease true Inferred relationship Some
Pelizaeus Merzbacher like disease due to AIMP1 mutation Associated morphology Dystrophy true Inferred relationship Some 1
Pelizaeus Merzbacher like disease due to AIMP1 mutation Finding site White matter structure of brain and spinal cord true Inferred relationship Some 1
Pelizaeus Merzbacher like disease due to AIMP1 mutation Finding site Myelinated nerve fibre structure true Inferred relationship Some 2
Pelizaeus Merzbacher like disease due to AIMP1 mutation Associated morphology Myelin sheath alteration true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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