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125495003: Myelin sheath alteration (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
193985010 Myelin sheath alteration en Synonym Active Entire term case insensitive SNOMED CT core module
729331011 Myelin sheath alteration (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myelin sheath alteration Is a Extracellular alteration true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Galactosylceramide beta-galactosidase deficiency Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Schultz disease Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Neuroaxonal leukodystrophy Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Type III transitional Pelizaeus-Merzbacher disease Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Type IV adult Pelizaeus-Merzbacher disease Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Type V atypical Pelizaeus-Merzbacher disease Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Type VI Cockayne Pelizaeus-Merzbacher disease Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Leucodystrophy without a known biochemical basis Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Globoid cell leukodystrophy, late-onset Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Dalmatian leukodystrophy Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Pelizaeus-Merzbacher disease, connatal variant Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Pelizaeus-Merzbacher disease Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Alexander's disease Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Pelizaeus-Merzbacher disease, classic form Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Leukodystrophy Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Leucodystrophy NOS Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Phytanic acid storage disease Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Pelizaeus-Merzbacher disease Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Pelizaeus-Merzbacher disease, connatal variant Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Phytanic acid storage disease Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Neuroaxonal leukodystrophy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Type V atypical Pelizaeus-Merzbacher disease Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Type IV adult Pelizaeus-Merzbacher disease Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Type III transitional Pelizaeus-Merzbacher disease Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Globoid cell leukodystrophy, late-onset Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Type VI Cockayne Pelizaeus-Merzbacher disease Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Pelizaeus-Merzbacher disease, classic form Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Leukodystrophy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Alexander's disease Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Schultz disease Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Dalmatian leukodystrophy Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Leucodystrophy without a known biochemical basis Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Leucodystrophy NOS Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Galactosylceramide beta-galactosidase deficiency Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Adult onset autosomal dominant leukodystrophy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Metachromatic leukodystrophy, adult type Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Ribonucleic acid polymerase III-related leukodystrophy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Progressive encephalopathy with severe infantile anorexia Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Pelizaeus Merzbacher like disease Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Cerebroretinal vasculopathy Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 3
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 6
Odontoleukodystrophy Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 3
X-linked spastic paraplegia type 2 Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 6
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 6
Ataxia co-occurrent and due to phytanic acid storage disease Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 5
Dermatoleukodystrophy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Odontoleukodystrophy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Tubulin beta 4A class IVa related leukodystrophy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Cerebroretinal vasculopathy Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Ataxia co-occurrent and due to phytanic acid storage disease Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 3
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 3
X-linked spastic paraplegia type 2 Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 3
Hypomyelination with brain stem and spinal cord involvement and leg spasticity Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Muscle eye brain disease with bilateral multicystic leukodystrophy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Galactocerebroside beta-galactosidase deficiency - early onset Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Pelizaeus Merzbacher like disease due to HSPD1 mutation Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Pelizaeus Merzbacher like disease due to SLC16A2 mutation Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Pelizaeus Merzbacher like disease due to AIMP1 mutation Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Pelizaeus Merzbacher like disease due to GJC2 mutation Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 2
Pelizaeus-Merzbacher disease null syndrome Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Pelizaeus-Merzbacher disease in female carrier Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Vanishing white matter disease Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Ovarioleukodystrophy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
C11ORF73-related autosomal recessive hypomyelinating leukodystrophy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
VPS11 core subunit of CORVET and HOPS complexes-related autosomal recessive hypomyelinating leukodystrophy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Multiple mitochondrial dysfunctions syndrome type 4 Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
4H leukodystrophy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Leukodystrophy due to alkaline ceramidase 3 deficiency Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Alexander disease juvenile form Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Alexander disease infantile form Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Alexander disease adult form Associated morphology True Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Leucodystrophy NOS Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1
Adult-onset autosomal dominant leucodystrophy Associated morphology False Myelin sheath alteration Inferred relationship Existential restriction modifier 1

This concept is not in any reference sets

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