13331008: atrophia (afwijkende morfologie)

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

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Noncystic peripheral retinal tuft (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Retinal detachment and occipital encephalocele	Associated morphology	True	Atrophy	Inferred relationship	Some	5
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Folliculitis cruris pustulosa atrophicans (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy of macula lutea	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Zonular traction peripheral retinal tuft (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	3
Atrophic fibrosis of lung	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Cogan-Reese syndrome (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Idiopathic atrophic hypothyroidism	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Lipoatrophy	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Widespread lipoatrophy (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Lipoatrophy caused by antiretroviral drug	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Lipodystrophia centrifugalis abdominalis infantalis	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Semicircular lipoatrophy	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Lipoatrophy caused by injected drug	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Lipoatrophy caused by injected corticosteroid	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Secondary vitreoretinal degeneration	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Wolfram syndrome	Associated morphology	True	Atrophy	Inferred relationship	Some	6
Insulin lipoatrophy	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Localised lipoatrophy	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Severe systemic illness-induced intestinal villous atrophy	Associated morphology	True	Atrophy	Inferred relationship	Some	3
Localised idiopathic lipoatrophy	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Lipoatrophy and lipodystrophy	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Vitiligo iridis	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Atrophy of iris of bilateral eyes (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy of iris of bilateral eyes (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Vitreoretinal tuft of bilateral eyes (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Vitreoretinal tuft of bilateral eyes (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Vitreoretinal tuft of bilateral eyes (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	3
Vitreoretinal tuft of bilateral eyes (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	4
Bilateral phthisis bulbi	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Bilateral phthisis bulbi	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Huntington's chorea	Associated morphology	True	Atrophy	Inferred relationship	Some	3
Juvenile onset Huntington's disease	Associated morphology	True	Atrophy	Inferred relationship	Some	5
Late onset Huntington's disease	Associated morphology	True	Atrophy	Inferred relationship	Some	5
Akinetic-rigid form of Huntington's disease	Associated morphology	True	Atrophy	Inferred relationship	Some	5
Atrophic nonflaccid left tympanic membrane	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophic nonflaccid right tympanic membrane (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy of muscle of bilateral forearms (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy of muscle of bilateral forearms (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Atrophy of muscle of right foot	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy of muscle of left foot (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy of muscle of right forearm (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy of muscle of left forearm (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy of muscle of bilateral upper arms (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy of muscle of bilateral upper arms (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Atrophy of muscle of bilateral thighs (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy of muscle of bilateral thighs (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Traumatic iris atrophy	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Idiopathic atrophy of nail in childhood (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Autosomal recessive Charcot-Marie-Tooth disease type 2	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Autosomal dominant Charcot-Marie-Tooth disease type 2	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Ocular anomalies, axonal neuropathy, developmental delay syndrome	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome	Associated morphology	True	Atrophy	Inferred relationship	Some	3
Autosomal dominant Charcot-Marie-Tooth disease type 2W	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Combined oxidative phosphorylation defect type 29	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Combined oxidative phosphorylation defect type 27	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Infantile inflammatory bowel disease with neurological involvement (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Charcot-Marie-Tooth disease type 2T (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Autosomal recessive Charcot-Marie-Tooth disease type 2X	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Autosomal dominant Charcot-Marie-Tooth disease type 2Z	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Autosomal dominant Charcot-Marie-Tooth disease type 2Y	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Charcot-Marie-Tooth disease type 2S	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Autosomal dominant Charcot-Marie-Tooth disease type 2V (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Autosomal dominant Charcot-Marie-Tooth disease type 2DD	Associated morphology	True	Atrophy	Inferred relationship	Some	1
DNAJB2-related Charcot-Marie-Tooth disease type 2	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Autosomal recessive isolated optic atrophy (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Autosomal recessive isolated optic atrophy (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Colobomatous optic disc, macular atrophy, chorioretinopathy syndrome	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Muscle atrophy of right ankle	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Muscle atrophy of left ankle	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Bilateral muscle atrophy of ankles	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Bilateral muscle atrophy of ankles	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Atrophy of muscle of bilateral shoulder regions (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy of muscle of bilateral shoulder regions (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Bilateral muscle atrophy of feet	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Bilateral muscle atrophy of feet	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Confetti-like atrophic macular lesions of skin (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Progressive cerebello-cerebral atrophy (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Progressive cerebello-cerebral atrophy (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Neurogenic scapuloperoneal syndrome Kaeser type (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Neurogenic scapuloperoneal syndrome Kaeser type (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Atrophy of multiple endocrine glands (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy of adrenal cortex (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Auditory neuropathy, optic atrophy syndrome (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy of globe of eye	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Phthisis bulbi	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Congenital peripapillary staphyloma	Associated morphology	True	Atrophy	Inferred relationship	Some	2
Congenital peripapillary staphyloma	Associated morphology	True	Atrophy	Inferred relationship	Some	3
Right globe atrophy	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Atrophy of left eye (disorder)	Associated morphology	True	Atrophy	Inferred relationship	Some	1
Placenta fenestrata	Associated morphology	True	Atrophy	Inferred relationship	Some	1

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Reference Sets

Dutch pathology simple reference set (foundation metadata concept)

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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
22798014	Atrophy, NOS	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT core
22799018	Simple atrophy	en	Synonym (core metadata concept)	Inactive	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
804561000146118	atrophia (afwijkende morfologie)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
804571000146112	atrophia	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
804581000146114	atrofie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
10305631000146118	Het afnemen in grootte en gewicht van weefsel, doordat cellen in aantal afnemen of doordat de functie van cellen afneemt.	nl	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)