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717042001: Pelizaeus Merzbacher like disease (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3308251012 Pelizaeus Merzbacher like disease (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3308252017 Pelizaeus Merzbacher like disease en Synonym Active Case sensitive SNOMED CT core
3308253010 PMLD - Pelizaeus Merzbacher like disease en Synonym Active Case sensitive SNOMED CT core
3308254016 An autosomal recessive leukodystrophy sharing identical clinical and radiological features as X-linked Pelizaeus-Merzbacher disease. Prevalence is unknown. It is characterized by early-onset nystagmus, delayed motor milestones, progressive spasticity, ataxia, and diffuse leukodystrophy on magnetic resonance imaging. en Definition Active Case sensitive SNOMED CT core
3308255015 An autosomal recessive leucodystrophy sharing identical clinical and radiological features as X-linked Pelizaeus-Merzbacher disease. Prevalence is unknown. It is characterised by early-onset nystagmus, delayed motor milestones, progressive spasticity, ataxia, and diffuse leucodystrophy on magnetic resonance imaging. en Definition Active Case sensitive SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pelizaeus Merzbacher like disease Is a Hereditary degenerative disease of central nervous system true Inferred relationship Some
Pelizaeus Merzbacher like disease Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Pelizaeus Merzbacher like disease Is a Leucodystrophy true Inferred relationship Some
Pelizaeus Merzbacher like disease Associated morphology Dystrophy false Inferred relationship Some 1
Pelizaeus Merzbacher like disease Associated morphology Myelin sheath alteration true Inferred relationship Some 1
Pelizaeus Merzbacher like disease Finding site Structure of nervous system false Inferred relationship Some 1
Pelizaeus Merzbacher like disease Finding site Myelinated nerve fibre structure true Inferred relationship Some 1
Pelizaeus Merzbacher like disease Associated morphology Dystrophy true Inferred relationship Some 2
Pelizaeus Merzbacher like disease Is a Hereditary disorder of nervous system false Inferred relationship Some
Pelizaeus Merzbacher like disease Finding site White matter structure of brain and spinal cord true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Pelizaeus Merzbacher like disease due to HSPD1 mutation Is a True Pelizaeus Merzbacher like disease Inferred relationship Some
Pelizaeus Merzbacher like disease due to SLC16A2 mutation Is a True Pelizaeus Merzbacher like disease Inferred relationship Some
Pelizaeus Merzbacher like disease due to AIMP1 mutation Is a True Pelizaeus Merzbacher like disease Inferred relationship Some
Pelizaeus Merzbacher like disease due to GJC2 mutation Is a True Pelizaeus Merzbacher like disease Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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