107669003: Degenerative abnormality (morphologic abnormality)

SNOMED CT Concept\Body structure (body structure)\Morphologically altered structure\Morphologically abnormal structure\Degenerative 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

172105010 Degenerative abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

593391011 Degenerative abnormality (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

65101000077112 anomalie dégénérative fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Degenerative abnormality	Is a	Morphologically abnormal structure	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
A rare disorder of fatty acid biosynthesis characterised by spastic paraparesis, bilateral congenital/juvenile cataracts, gross motor developmental delay, speech delay and truncal hypotonia. Seizures in infancy can also be observed. Patients have elevated levels of ether lipids including plasmalogen. Majority of the affected individuals have normal brain imaging and normal growth. No microcephaly or dysmorphic features were reported.	Associated morphology	True	Degenerative abnormality	Inferred relationship	Some	1
Early onset dementia due to Lewy body disease (disorder)	Associated morphology	True	Degenerative abnormality	Inferred relationship	Some	1
Early onset dementia due to Lewy body disease (disorder)	Associated morphology	True	Degenerative abnormality	Inferred relationship	Some	2
Dementia due to Lewy body disease	Associated morphology	True	Degenerative abnormality	Inferred relationship	Some	1
Dementia due to Lewy body disease	Associated morphology	True	Degenerative abnormality	Inferred relationship	Some	2
GRN-related frontotemporal dementia	Associated morphology	True	Degenerative abnormality	Inferred relationship	Some	2
Early-onset neurodegeneration, choreoathetoid movement, microcytic anemia due to iron responsive element binding protein 2 gene mutation (disorder)	Associated morphology	True	Degenerative abnormality	Inferred relationship	Some	1

Start Previous Page 17 of 17

This concept is not in any reference sets