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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
Cutaneous atrophy caused by corticosteroids (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of skin caused by drug (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Secondary anetoderma Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Drug-induced cutis laxa (disorder) Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Atrophy of gallbladder Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Generalised iris atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophic-hyperplastic gastritis Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
Roussy-Levy syndrome Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of breast Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of corpus cavernosum Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Stringhalt Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Onychoatrophy due to lichen planus (disorder) Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of bile duct Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Chronic yellow atrophy of liver Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Acne atrophica (disorder) Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Localized abdominal wall skin atrophy Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Wolfram syndrome (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyotrophy caused by herpes zoster Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Muscle atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophic scarring of cheeks Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Pancreatic acinar atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of pancreas Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophic thrush Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Neuralgic amyotrophy (disorder) Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Roussy-Lévy syndrome Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Neuralgic amyotrophy (disorder) Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
Late cortical cerebellar atrophy Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of skeletal muscle of pelvis (disorder) Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of epithelium (morphologic abnormality) Is a True Atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Glaucomatous atrophy of optic disc (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of skeletal muscle of pelvis (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Zahn's infarct Is a True Atrophy Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebellar cortical atrophy (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital atrophy of thyroid Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital renal atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital atrophy of left lobe of liver Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Amyotrophia congenita Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital ischaemic atrophy of central nervous system structure Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
Retinal detachment and occipital encephalocele Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 9
Localised lipoatrophy Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Localised idiopathic lipoatrophy Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Semicircular lipoatrophy Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Lipodystrophia centrifugalis abdominalis infantalis Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Post-inflammatory lipoatrophy Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
A rare localised lipodystrophy characterised by the appearance of asymptomatic, well-demarcated, variably sized, depressed, lipoatrophic lesions secondary to subcutaneous, intradermic or intramuscular drug injection, including corticosteroids, insulin, human growth hormone and antibiotics. Skin colouration may vary from white or hypopigmented to reddish, pinkish or violaceous. Epidermal atrophy may be also present. Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Insulin lipoatrophy Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Lipoatrophy Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Severe malnutrition due to type 2 diabetes mellitus Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Acquired generalized lipodystrophy Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Severe malnutrition due to type 1 diabetes mellitus Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Lipoatrophy due to Human immunodeficiency virus infection and treatment Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Ozena laryngis Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 4
Amyotrophia congenita Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Gyrate atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
Idiopathic atrophoderma of Pasini and Pierini Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
Lipoatrophy caused by antiretroviral drug Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophic endometritis Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Choroideremia co-occurrent with hypopituitarism Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
Altered behavior due to Pick's disease (disorder) Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 4
Behr syndrome Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant Charcot-Marie-Tooth disease type 2B (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by distal weakness primarily and predominantly occurring in the upper limbs and tendon reflexes absent or reduced in the arms and decreased in the legs. Progression is slow. Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, with onset in the first to 6th decade with a gait anomaly and a leg weakness that reaches the arms secondarily. Tendon reflexes are reduced or absent and, after years, all patients have a pes cavus. Other signs may be present, including hearing loss and postural tremor. Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant Charcot-Marie-Tooth disease type 2I (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant Charcot-Marie-Tooth disease type 2J (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant Charcot-Marie-Tooth disease type 2A1 (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 4
Atrophy of quadriceps femoris muscle (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of trapezius muscle (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of temporalis muscle (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of pectoral muscle (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of latissimus dorsi muscle (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of interosseous muscle of hand (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of gluteus maximus muscle (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of gastrocnemius muscle (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophy of deltoid muscle Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by symmetric weakness primarily occurring in the lower limbs (distal muscles in a majority of cases) and reaching the arms only after 5 to 10 years, occasional and predominantly distal sensory loss and reduced tendon reflexes. It presents with gait anomaly between the 1st and 6th decade and early onset is generally associated to a more severe phenotype which may include foot drop. Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant Charcot-Marie-Tooth disease type 2G (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant Charcot-Marie-Tooth disease type 2K (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. In the single family reported to date, CMT2L onset is between 15 and 33 years. Patients present with a symmetric distal weakness of legs and occasionally of the hands, absent or reduced tendon reflexes, distal legs sensory loss and frequently a pes cavus. Progression is slow. Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant Charcot-Marie-Tooth disease type 2M (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant Charcot-Marie-Tooth disease type 2N (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Charcot-Marie-Tooth disease type 2B2 Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Microphthalmia with brain atrophy syndrome (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Microphthalmia with brain atrophy syndrome (disorder) Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
Annular atrophic lichen planus (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Charcot-Marie-Tooth disease type 2H Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Choroidal atrophy (finding) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Choroidal atrophy and alopecia syndrome (disorder) Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 5
Cerebral atrophy (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Rombo syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Phthisis bulbi of left eye (disorder) Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Phthisis bulbi of right eye (disorder) Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Intellectual disability, developmental delay, contracture syndrome Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 3
Severe X-linked intellectual disability Gustavson type (disorder) Associated morphology False Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 5
Atrophy of soft tissue of orbit (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital atrophy of optic nerve (disorder) Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 1
Post poliomyelitis syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Chorioretinal atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 2
Chorioretinal atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier (core metadata concept) 3

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