111007000: Hypomyelination (morphologic abnormality)

SNOMED CT Concept\Body structure\Morphologically altered structure\Morphologically abnormal structure\Hypomyelination

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

175932012 Hypomyelination en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

627344012 Hypomyelination (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

175932012 Hypomyelination en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

175932012 Hypomyelination en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

627344012 Hypomyelination (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

627344012 Hypomyelination (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hypomyelination	Is a	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypomyelination	Is a	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder)	Associated morphology	False	Hypomyelination	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Epileptic encephalopathy with global cerebral demyelination (disorder)	Associated morphology	False	Hypomyelination	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hypomyelination neuropathy arthrogryposis syndrome (disorder)	Associated morphology	True	Hypomyelination	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Epileptic encephalopathy with global cerebral demyelination (disorder)	Associated morphology	True	Hypomyelination	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hypomyelinating neuropathy	Associated morphology	True	Hypomyelination	Inferred relationship	Existential restriction modifier (core metadata concept)	1
MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome	Associated morphology	True	Hypomyelination	Inferred relationship	Existential restriction modifier (core metadata concept)	5

This concept is not in any reference sets