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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
1083641000241115 atrophie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

50 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Atrophy Is a Degenerative abnormality false Inferred relationship Some
Atrophy Is a dégénérescence false Inferred relationship Some
Atrophy Is a Degenerative abnormality true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Cutaneous atrophy caused by corticosteroids Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of skin caused by drug (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Secondary anetoderma Associated morphology False Atrophy Inferred relationship Some 1
Drug-induced cutis laxa (disorder) Associated morphology False Atrophy Inferred relationship Some 2
Atrophy of gallbladder Associated morphology True Atrophy Inferred relationship Some 1
Generalized iris atrophy (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophic-hyperplastic gastritis Associated morphology True Atrophy Inferred relationship Some 3
Roussy-Levy syndrome Associated morphology False Atrophy Inferred relationship Some 1
Atrophy of breast Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of corpus cavernosum Associated morphology True Atrophy Inferred relationship Some 1
Stringhalt Associated morphology False Atrophy Inferred relationship Some 1
Onychoatrophy due to lichen planus (disorder) Associated morphology False Atrophy Inferred relationship Some 1
Atrophy of bile duct Associated morphology True Atrophy Inferred relationship Some 1
Chronic yellow atrophy of liver Associated morphology False Atrophy Inferred relationship Some 1
Acne atrophica Associated morphology False Atrophy Inferred relationship Some 2
Localized abdominal wall skin atrophy Associated morphology False Atrophy Inferred relationship Some 1
A rare, genetic, endocrine disorder characterised by type I diabetes mellitus (DM), diabetes insipidus (DI), sensorineural deafness (D), bilateral optical atrophy (OA) and neurological signs. Associated morphology True Atrophy Inferred relationship Some 1
Amyotrophy caused by herpes zoster Associated morphology True Atrophy Inferred relationship Some 1
Muscle atrophy Associated morphology True Atrophy Inferred relationship Some 1
Atrophic scarring of cheeks Associated morphology False Atrophy Inferred relationship Some 1
Pancreatic acinar atrophy Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of pancreas Associated morphology True Atrophy Inferred relationship Some 1
Atrophic thrush Associated morphology False Atrophy Inferred relationship Some 1
Neuralgic amyotrophy Associated morphology False Atrophy Inferred relationship Some 2
Roussy-Lévy syndrome Associated morphology False Atrophy Inferred relationship Some 2
Neuralgic amyotrophy Associated morphology False Atrophy Inferred relationship Some 3
Late cortical cerebellar atrophy Associated morphology False Atrophy Inferred relationship Some 1
Atrophy of skeletal muscle of pelvis (disorder) Associated morphology False Atrophy Inferred relationship Some 1
Atrophy of epithelium (morphologic abnormality) Is a True Atrophy Inferred relationship Some
Glaucomatous atrophy of optic disc Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of skeletal muscle of pelvis (disorder) Associated morphology True Atrophy Inferred relationship Some 1
An area of pseudoinfarction with congestion and parenchymal atrophy but no infarction Is a True Atrophy Inferred relationship Some
Congenital cerebellar cortical atrophy (disorder) Associated morphology True Atrophy Inferred relationship Some 2
Congenital atrophy of thyroid Associated morphology True Atrophy Inferred relationship Some 2
Congenital renal atrophy Associated morphology True Atrophy Inferred relationship Some 2
Congenital atrophy of left lobe of liver Associated morphology True Atrophy Inferred relationship Some 2
Amyotrophia congenita Associated morphology False Atrophy Inferred relationship Some 3
Congenital ischemic atrophy of central nervous system structure Associated morphology True Atrophy Inferred relationship Some 3
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. Associated morphology True Atrophy Inferred relationship Some 9
Localised lipoatrophy Associated morphology False Atrophy Inferred relationship Some 2
Localized idiopathic lipoatrophy Associated morphology False Atrophy Inferred relationship Some 2
Semicircular lipoatrophy Associated morphology False Atrophy Inferred relationship Some 2
Lipodystrophia centrifugalis abdominalis infantalis Associated morphology False Atrophy Inferred relationship Some 2
Post-inflammatory lipoatrophy Associated morphology False Atrophy Inferred relationship Some 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 Some 2
Insulin lipoatrophy Associated morphology False Atrophy Inferred relationship Some 2
Lipoatrophy Associated morphology False Atrophy Inferred relationship Some 1
Severe malnutrition due to type 2 diabetes mellitus Associated morphology False Atrophy Inferred relationship Some 2
Acquired generalized lipodystrophy Associated morphology False Atrophy Inferred relationship Some 2
Severe malnutrition due to type 1 diabetes mellitus (disorder) Associated morphology False Atrophy Inferred relationship Some 2
Lipoatrophy due to Human immunodeficiency virus infection and treatment Associated morphology False Atrophy Inferred relationship Some 2
Ozena laryngis Associated morphology True Atrophy Inferred relationship Some 4
Amyotrophia congenita Associated morphology True Atrophy Inferred relationship Some 2
Gyrate atrophy Associated morphology True Atrophy Inferred relationship Some 3
Idiopathic atrophoderma of Pasini and Pierini Associated morphology True Atrophy Inferred relationship Some 3
Lipoatrophy caused by antiretroviral drug Associated morphology False Atrophy Inferred relationship Some 1
Atrophic endometritis Associated morphology True Atrophy Inferred relationship Some 2
Choroideremia co-occurrent with hypopituitarism Associated morphology False Atrophy Inferred relationship Some 3
Altered behavior due to Pick's disease (disorder) Associated morphology False Atrophy Inferred relationship Some 4
Behr syndrome Associated morphology False Atrophy Inferred relationship Some 1
A severe form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, with onset in the 2nd or 3rd decade, characterized by ulcerations and infections of feet. Symmetric and distal weakness develops mostly in the legs together with a severe symmetric distal sensory loss, tendon reflexes are only reduced at ankles and foot deformities, including pes cavus or planus and hammer toes, appear in childhood. Associated morphology True Atrophy Inferred relationship Some 2
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by the association of vocal cord anomalies, impairment of respiratory muscles and sensorineural hearing loss with the distal hands and feet weakness. Onset is between infancy and the 6th decade. Associated morphology True Atrophy Inferred relationship Some 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 Some 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 Some 2
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by a late onset with severe sensory loss (paresthesia and hypoesthesia) associated with distal weakness, mainly of the legs, and absent or reduced deep tendon reflexes. Associated morphology True Atrophy Inferred relationship Some 2
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by a relatively late onset, pupillary abnormalities and deafness, in most patients, associated with distal weakness and muscle atrophy. Associated morphology True Atrophy Inferred relationship Some 2
Autosomal dominant Charcot-Marie-Tooth disease type 2A1 (disorder) Associated morphology True Atrophy Inferred relationship Some 2
An X-linked syndromic intellectual disability characterized by intellectual disability, subcortical cerebral atrophy, dental anomalies, patella luxation, lower back skin dimple, and dysmorphic facial features. Associated morphology False Atrophy Inferred relationship Some 4
Atrophy of quadriceps femoris muscle (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of trapezius muscle (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of temporalis muscle (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of pectoral muscle (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of latissimus dorsi muscle (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of interosseous muscle of hand (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of gluteus maximus muscle (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of gastrocnemius muscle (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of deltoid muscle (disorder) Associated morphology True Atrophy Inferred relationship Some 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 Some 2
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy with onset associated to development of foot deformity and walking difficulties between the 1st and the 8th decades, with a median range in the 2nd one. Weakness and sensory loss involve primarily the legs and ankles tendon reflexes are reduced. This disorder has a slowly progressive course. Associated morphology True Atrophy Inferred relationship Some 2
An axonal Charcot-Marie-Tooth (CMT) peripheral sensorimotor polyneuropathy. Associated morphology True Atrophy Inferred relationship Some 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 Some 2
A form of axonal Charcot-Marie-Tooth disease, a peripheral motor and sensory neuropathy, characterized by congenital ptosis and early cataract associated to a mildly progressive peripheral neuropathy of variable onset from birth to the 6th decade, pes cavus, reduced to absent ankles tendon reflexes and sometimes neutropenia. Associated morphology True Atrophy Inferred relationship Some 2
A mild form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by distal legs sensory loss and weakness that can be asymmetric. Tendon reflexes are reduced in the knees and absent in ankles. Progression is slow. Associated morphology True Atrophy Inferred relationship Some 2
Charcot-Marie-Tooth disease, type 2B2 (CMT2B2, also referred to as CMT4C3) is an axonal CMT peripheral sensorimotor polyneuropathy that has been described in a large consanguineous Costa Rican family of Spanish ancestry. Associated morphology True Atrophy Inferred relationship Some 2
A rare genetic neurodegenerative disorder characterized by congenital microphthalmia, sunken eyes, blindness, microcephaly, severe intellectual disability, progressive spasticity, and seizures. Psychomotor development is normal in the first 6-8 months of life and thereafter declines rapidly and continuously. Brain MRI reveals progressive and extensive degenerative changes, especially cortex, cerebellum, brainstem, and corpus callosum atrophy, with complete loss of cerebral white matter. Associated morphology True Atrophy Inferred relationship Some 2
A rare genetic neurodegenerative disorder characterized by congenital microphthalmia, sunken eyes, blindness, microcephaly, severe intellectual disability, progressive spasticity, and seizures. Psychomotor development is normal in the first 6-8 months of life and thereafter declines rapidly and continuously. Brain MRI reveals progressive and extensive degenerative changes, especially cortex, cerebellum, brainstem, and corpus callosum atrophy, with complete loss of cerebral white matter. Associated morphology False Atrophy Inferred relationship Some 3
A rare variant of cutaneous lichen planus characterized by both annular and atrophic LP features in the same lesion. Associated morphology True Atrophy Inferred relationship Some 1
Charcot-Marie-Tooth disease, type 2H (CMT2H, also referred to as CMT4C2) is an axonal CMT peripheral sensorimotor polyneuropathy associated with pyramidal involvement. Associated morphology True Atrophy Inferred relationship Some 2
Choroidal atrophy Associated morphology True Atrophy Inferred relationship Some 1
A rare ectodermal dysplasia syndrome, characterized by the association of choroidal atrophy (sometimes regional), together with other ectodermal dysplasia features including fine and sparse hair, absent or decreased lashes and eyebrows, and possibly mild visual loss and dysplastic/thick/grooved nails. Associated morphology False Atrophy Inferred relationship Some 5
Cerebral atrophy Associated morphology True Atrophy Inferred relationship Some 1
Rombo syndrome is characterized by vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, peripheral vasodilation with cyanosis and basal cell carcinomas. Associated morphology True Atrophy Inferred relationship Some 2
Phthisis bulbi of left eye (disorder) Associated morphology False Atrophy Inferred relationship Some 2
Phthisis bulbi of right eye (disorder) Associated morphology False Atrophy Inferred relationship Some 2
Intellectual disability-developmental delay-contractures syndrome, formerly known as Wieacker-Wolff syndrome, is a severe X-linked recessive neurodevelopmental disorder characterized by severe contractures and intellectual disability. Associated morphology False Atrophy Inferred relationship Some 3
A rare, genetic, X-linked syndromic intellectual disability disorder characterized by severe intellectual disability, microcephaly, post-natal growth retardation, severe visual impairment or blindness (due to optic atrophy), severe hearing defect, spasticity, epileptic seizures, restricted large-joint movements and early death (in infancy or early childhood). Facial dysmorphic features (large dysplastic ears and short broad nose) are additionally observed. There have been no further descriptions in the literature since 1993. Associated morphology False Atrophy Inferred relationship Some 5
Atrophy of soft tissue of orbit (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Congenital atrophy of optic nerve (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Post poliomyelitis syndrome Associated morphology True Atrophy Inferred relationship Some 2
Chorioretinal atrophy Associated morphology True Atrophy Inferred relationship Some 2
Chorioretinal atrophy Associated morphology True Atrophy Inferred relationship Some 3

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