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125495003: Myelin sheath alteration (morphologic abnormality)


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

Descriptions:

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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myelin sheath alteration Is a Extracellular alteration (morphologic abnormality) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Multiple mitochondrial dysfunctions syndrome type 5 (disorder) Associated morphology True Myelin sheath alteration Inferred relationship Some 1
Atypical Krabbe disease due to saposin A deficiency (disorder) Associated morphology True Myelin sheath alteration Inferred relationship Some 1
Cholestanol storage disease Associated morphology True Myelin sheath alteration Inferred relationship Some 1
MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome Associated morphology True Myelin sheath alteration Inferred relationship Some 1
Hypomyelination of early myelinating structures (disorder) Associated morphology True Myelin sheath alteration Inferred relationship Some 1
Alexander disease type II Associated morphology True Myelin sheath alteration Inferred relationship Some 1

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Reference Sets

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