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447351004: Vanishing white matter disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2011. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2880283014 Vanishing white matter disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2883499019 Vanishing white matter disease en Synonym Active Entire term case insensitive SNOMED CT core module
4551991015 Myelinosis centralis diffusa en Synonym Active Entire term case insensitive SNOMED CT core module
4551992010 Childhood ataxia with diffuse central nervous system hypomyelination en Synonym Active Entire term case insensitive SNOMED CT core module
4551993017 CACH (childhood ataxia with diffuse central nervous system hypomyelination) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
4551994011 Leucoencephalopathy with vanishing white matter en Synonym Active Entire term case insensitive SNOMED CT core module
4551995012 Leukoencephalopathy with vanishing white matter en Synonym Active Entire term case insensitive SNOMED CT core module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Vanishing white matter disease Is a Disorder of brain false Inferred relationship Existential restriction modifier
Vanishing white matter disease Is a Demyelinating disease of central nervous system false Inferred relationship Existential restriction modifier
Vanishing white matter disease Associated morphology Demyelination false Inferred relationship Existential restriction modifier 1
Vanishing white matter disease Finding site Cerebral white matter structure false Inferred relationship Existential restriction modifier 1
Vanishing white matter disease Associated morphology Demyelination false Inferred relationship Existential restriction modifier 1
Vanishing white matter disease Finding site Cerebral white matter structure false Inferred relationship Existential restriction modifier 1
Vanishing white matter disease Is a White matter disease false Inferred relationship Existential restriction modifier
Vanishing white matter disease Associated morphology Myelin sheath alteration true Inferred relationship Existential restriction modifier 1
Vanishing white matter disease Is a Hereditary ataxia true Inferred relationship Existential restriction modifier
Vanishing white matter disease Is a Cerebral degeneration true Inferred relationship Existential restriction modifier
Vanishing white matter disease Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Vanishing white matter disease Finding site Cerebral white matter structure true Inferred relationship Existential restriction modifier 2
Vanishing white matter disease Finding site Myelinated nerve fiber structure true Inferred relationship Existential restriction modifier 1
Vanishing white matter disease Is a Leukoencephalopathy true Inferred relationship Existential restriction modifier
Vanishing white matter disease Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Vanishing white matter disease Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 2
Vanishing white matter disease Is a Leukodystrophy true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Ovarioleukodystrophy Is a True Vanishing white matter disease Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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