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13331008: Atrophy (morphologic abnormality)

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

Descriptions:

Id Description Lang Type Status Case? Module
22797016 Atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
737978016 Atrophy (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1220945019 Atrophic en Synonym Active Entire term case insensitive SNOMED CT core module

41 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Atrophy Is a Degenerative abnormality false Inferred relationship Existential restriction modifier
Atrophy Is a Degeneration false Inferred relationship Existential restriction modifier
Atrophy Is a Degenerative abnormality true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Noncystic peripheral retinal tuft Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Retinal detachment and occipital encephalocele Associated morphology True Atrophy Inferred relationship Existential restriction modifier 5
Autosomal dominant neovascular inflammatory vitreoretinopathy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Folliculitis cruris pustulosa atrophicans Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of macula lutea Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Zonular traction peripheral retinal tuft Associated morphology True Atrophy Inferred relationship Existential restriction modifier 3
Atrophic fibrosis of lung Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Cogan-Reese syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Idiopathic atrophic hypothyroidism Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Lipoatrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Widespread lipoatrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Lipoatrophy caused by antiretroviral drug Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Lipodystrophia centrifugalis abdominalis infantalis Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Semicircular lipoatrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Lipoatrophy caused by injected drug Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Lipoatrophy caused by injected corticosteroid Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Secondary vitreoretinal degeneration Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Diabetes mellitus AND insipidus with optic atrophy AND deafness Associated morphology True Atrophy Inferred relationship Existential restriction modifier 6
Insulin lipoatrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Localized lipoatrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Severe systemic illness-induced intestinal villous atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 3
Localized idiopathic lipoatrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Lipoatrophy and lipodystrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Vitiligo iridis Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Atrophy of iris of bilateral eyes Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of iris of bilateral eyes Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Vitreoretinal tuft of bilateral eyes Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Vitreoretinal tuft of bilateral eyes Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Vitreoretinal tuft of bilateral eyes Associated morphology True Atrophy Inferred relationship Existential restriction modifier 3
Vitreoretinal tuft of bilateral eyes Associated morphology True Atrophy Inferred relationship Existential restriction modifier 4
Phthisis bulbi of bilateral eyes Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Phthisis bulbi of bilateral eyes Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Huntington's chorea Associated morphology True Atrophy Inferred relationship Existential restriction modifier 3
Juvenile onset Huntington's disease Associated morphology True Atrophy Inferred relationship Existential restriction modifier 5
Late onset Huntington's disease Associated morphology True Atrophy Inferred relationship Existential restriction modifier 5
Akinetic-rigid form of Huntington's disease Associated morphology True Atrophy Inferred relationship Existential restriction modifier 5
Atrophic nonflaccid left tympanic membrane Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophic nonflaccid right tympanic membrane Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of bilateral forearms Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of bilateral forearms Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Atrophy of muscle of right foot Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of left foot Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of right forearm Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of left forearm Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of bilateral upper arms Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of bilateral upper arms Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Atrophy of muscle of bilateral thighs Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of bilateral thighs Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Traumatic iris atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Idiopathic atrophy of nail in childhood Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal recessive Charcot-Marie-Tooth disease type 2 Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2 Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Ocular anomalies, axonal neuropathy, developmental delay syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 3
Autosomal dominant Charcot-Marie-Tooth disease type 2W Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to diacylglycerol O-acyltransferase 2 mutation Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Combined oxidative phosphorylation defect type 29 Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Combined oxidative phosphorylation defect type 27 Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Infantile inflammatory bowel disease with neurological involvement Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Charcot-Marie-Tooth disease type 2T Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal recessive Charcot-Marie-Tooth disease type 2X Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Autosomal dominant Charcot-Marie-Tooth disease type 2Z Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2Y Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to trafficking from endoplasmic reticulum to golgi regulator mutation Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Charcot-Marie-Tooth disease type 2S Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2V Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2DD Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
DnaJ heat shock protein family (Hsp40) member B2-related Charcot-Marie-Tooth disease type 2 Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal recessive isolated optic atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal recessive isolated optic atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Colobomatous optic disc, macular atrophy, chorioretinopathy syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle acting on right ankle joint Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle acting on left ankle joint Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle acting on bilateral ankle joints Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle acting on bilateral ankle joints Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Atrophy of muscle of bilateral shoulder regions Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of bilateral shoulder regions Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Atrophy of muscle of bilateral feet Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of bilateral feet Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Confetti-like atrophic macular lesions of skin Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Progressive cerebello-cerebral atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Progressive cerebello-cerebral atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Neurogenic scapuloperoneal syndrome Kaeser type Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Neurogenic scapuloperoneal syndrome Kaeser type Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Atrophy of multiple endocrine glands Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of adrenal cortex Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Auditory neuropathy, optic atrophy syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of globe of eye Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Phthisis bulbi Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Congenital peripapillary staphyloma Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Congenital peripapillary staphyloma Associated morphology True Atrophy Inferred relationship Existential restriction modifier 3
Atrophy of right eye Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of left eye Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Placenta fenestrata Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1

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