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13331008: Atrophy (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
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
22797016 Atrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
22797016 Atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
22799018 Simple atrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
22799018 Simple 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 Only initial character 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 Only initial character 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
1083641000241115 atrophie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1083641000241115 atrophie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

43 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Atrophy Is a Degenerative abnormality (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept)
Atrophy Is a dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept)
Atrophy Is a Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Placenta fenestrata Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
NAD(P)HX dehydratase deficiency Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophic cervicitis (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Benign monomelic amyotrophy of lower limb Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Benign monomelic amyotrophy of upper limb (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Spinocerebellar ataxia type 45 (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Acquired cerebellar atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare genetic endocrine disorder with characteristics of type 1 diabetes mellitus (DM), diabetes insipidus (DI), sensorineural deafness (D), bilateral optical atrophy (OA) and neurological signs. Type 1 has onset in the first decade with diabetes mellitus and optic atrophy manifestations. 50% of patients also develop diabetes insipidus. Additional features may include urinary tract abnormalities, neurological involvement and psychiatric manifestations. Caused by caused by homozygous or compound heterozygous mutation in the gene encoding wolframin (WFS1) on chromosome 4p16. Transmission is autosomal recessive. Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare genetic endocrine disorder with characteristics of type 1 diabetes mellitus (DM), diabetes insipidus (DI), sensorineural deafness (D), bilateral optical atrophy (OA) and neurological signs. Type 1 has onset in the first decade with diabetes mellitus and optic atrophy manifestations. 50% of patients also develop diabetes insipidus. Additional features may include urinary tract abnormalities, neurological involvement and psychiatric manifestations. Caused by caused by homozygous or compound heterozygous mutation in the gene encoding wolframin (WFS1) on chromosome 4p16. Transmission is autosomal recessive. Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Wolfram syndrome type 2 Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Wolfram syndrome type 2 Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Nongeographic atrophy of macula Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Denture stomatitis Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 4
Chronic atrophic candidosis (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Phthisis bulbi of left eye (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Phthisis bulbi of right eye (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Necrobiosis lipoidica, granulomatous type Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
Necrobiosis lipoidica diabeticorum Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
Granulomatosis disciformis et progressiva Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 4
Necrobiosis lipoidica, necrobiotic type Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
Necrobiosis lipoidica Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
Right orbital atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of left orbit (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of bilateral orbits (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of bilateral orbits (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Essential iris atrophy of bilateral eyes (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Essential iris atrophy of bilateral eyes (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Essential iris atrophy of right eye (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Essential iris atrophy of left eye (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of bilateral eyes Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of bilateral eyes Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Atrophy of optic disc of left eye due to glaucoma Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of optic disc of right eye due to glaucoma (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of optic disc of bilateral eyes due to glaucoma (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of optic disc of bilateral eyes due to glaucoma (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Atrophia cutis senilis (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophic scar (morphologic abnormality) Is a True Atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Dermal elastolysis Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atypical Krabbe disease due to saposin A deficiency (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Elastoderma Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
O'Sullivan McLeod syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Central papillary atrophy of tongue (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atelectasis of tympanic membrane due to chronic otitis media with effusion (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Atelectasis of tympanic membrane due to adhesive otitis media Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Tympanic atelectasis Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophic Hashimoto thyroiditis Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1

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