13331008: Atrophy (morphologic abnormality)

SNOMED CT Concept\Body structure\Morphologically altered structure\Morphologically abnormal structure (morphologic abnormality)\Degenerative abnormality (morphologic abnormality)\Atrophy

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

22797016 Atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

737978016 Atrophy (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1220945019 Atrophic en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

7501000052114 atrofi sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Atrophy	Is a	Degenerative abnormality (morphologic abnormality)	false	Inferred relationship	Some
Atrophy	Is a	degeneration	false	Inferred relationship	Some
Atrophy	Is a	Degenerative abnormality (morphologic abnormality)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Placenta fenestrata	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
NAD(P)HX dehydratase deficiency (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophic cervicitis (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Benign monomelic amyotrophy of lower limb (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Benign monomelic amyotrophy of upper limb (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Spinocerebellar ataxia type 45 (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Acquired cerebellar atrophy	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Wolfram syndrome type 1 (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Wolfram syndrome type 1 (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Wolfram syndrome type 2	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Wolfram syndrome type 2	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Nongeographic atrophy of macula	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophic vaginal mucosa (finding)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Huntington's chorea with hyperactive behavior (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	3

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This concept is not in any reference sets