125495003: verandering van myelineschede (afwijkende morfologie)

SNOMED CT Concept\Body structure\Morphologically altered structure\Morphologically abnormal structure (morphologic abnormality)\Lesion (morphologic abnormality)\Extracellular alteration (morphologic abnormality)\Myelin sheath alteration

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
1245671000146111 verandering van myelineschede nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
1245681000146113 verandering van myelineschede (afwijkende morfologie) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
1802661000146110 mergschedeverandering nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

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
Atypical phytanic acid storage disease (disorder)	Associated morphology	True	Myelin sheath alteration	Inferred relationship	Some	3

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