FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

107669003: Degenerative abnormality (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
172105010 Degenerative abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
593391011 Degenerative abnormality (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
65101000077112 anomalie dégénérative fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

201 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Degenerative abnormality Is a Morphologically abnormal structure true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Bilateral tendinosis of wrists Associated morphology True Degenerative abnormality Inferred relationship Some 2
Tendinosis of wrist region (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of bilateral elbows Associated morphology False Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of bilateral elbows Associated morphology False Degenerative abnormality Inferred relationship Some 2
Secondary osteoarthritis of right elbow Associated morphology False Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of elbow Associated morphology False Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of left elbow Associated morphology False Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of joint of right knee (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of left knee Associated morphology False Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of bilateral knees Associated morphology False Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of bilateral knees Associated morphology False Degenerative abnormality Inferred relationship Some 2
Secondary osteoarthritis of left glenohumeral joint (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of right glenohumeral joint (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of bilateral glenohumeral joints (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of bilateral glenohumeral joints (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 2
Secondary osteoarthritis of left hip joint (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of right hip joint (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of bilateral hips Associated morphology False Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of bilateral hips Associated morphology False Degenerative abnormality Inferred relationship Some 2
Secondary osteoarthritis of hip joint (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 1
Secondary osteoarthritis of glenohumeral joint Associated morphology False Degenerative abnormality Inferred relationship Some 1
Tendinosis of elbow region (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Tendinosis of shoulder region Associated morphology True Degenerative abnormality Inferred relationship Some 1
Tendinosis of foot (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Tendinosis of ankle region (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Tendinosis of knee region (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Degenerative disorder of left eye (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Degenerative disorder of right eye Associated morphology True Degenerative abnormality Inferred relationship Some 1
Degenerative disorder of bilateral eyes (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Degenerative disorder of bilateral eyes (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 2
Congenital chorioretinal degeneration of left eye (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Congenital chorioretinal degeneration of left eye (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 2
Congenital chorioretinal degeneration of right eye Associated morphology True Degenerative abnormality Inferred relationship Some 1
Congenital chorioretinal degeneration of right eye Associated morphology True Degenerative abnormality Inferred relationship Some 2
Congenital chorioretinal degeneration of bilateral eyes Associated morphology True Degenerative abnormality Inferred relationship Some 1
Congenital chorioretinal degeneration of bilateral eyes Associated morphology True Degenerative abnormality Inferred relationship Some 2
Congenital chorioretinal degeneration of bilateral eyes Associated morphology True Degenerative abnormality Inferred relationship Some 3
Congenital chorioretinal degeneration of bilateral eyes Associated morphology True Degenerative abnormality Inferred relationship Some 4
Degeneration of ciliary body of left eye (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Degeneration of ciliary body of right eye (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Degeneration of ciliary body of bilateral eyes (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Degeneration of ciliary body of bilateral eyes (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 2
Osteoarthritis of right acromioclavicular joint (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 1
Osteoarthritis of left acromioclavicular joint (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 1
Disciform macular degeneration (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Forster-Fuchs spot of bilateral eyes Associated morphology True Degenerative abnormality Inferred relationship Some 1
Forster-Fuchs spot of bilateral eyes Associated morphology True Degenerative abnormality Inferred relationship Some 2
Forster-Fuchs spot of right eye (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Forster-Fuchs spot of left eye (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Vitamin A deficiency with keratomalacia (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Keratomalacia of left eye (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Right keratomalacia Associated morphology True Degenerative abnormality Inferred relationship Some 1
Keratomalacia of bilateral eyes (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Keratomalacia of bilateral eyes (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 2
Keratomalacia Associated morphology True Degenerative abnormality Inferred relationship Some 1
An autosomal recessive neurodegenerative disorder with a variable age at onset in the first years of life after normal early development followed by decline of mental and motor capacities, epilepsy, and vision loss through retinal degeneration. Caused by homozygous or compound heterozygous mutation in the CLN6 gene on chromosome 15q23. Associated morphology True Degenerative abnormality Inferred relationship Some 1
Degenerative disorder of articular cartilage of knee (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Degenerative disorder of articular cartilage of left knee (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Degenerative disorder of articular cartilage of right knee (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
A rare genetic neurological disorder with characteristics of childhood onset of severe global neurodevelopmental regression with eventual loss of independent walking and loss of language and fine and gross motor skills, and development of severe dysphagia requiring tube feeding, seizures, cerebellar syndrome, dystonia, and other neurologic manifestations. Brain imaging shows progressive cerebral and/or cerebellar atrophy in most cases. A less severe phenotype associated with missense mutations shows no regression or movement abnormalities, ambulation is preserved, and brain imaging is normal. Associated morphology True Degenerative abnormality Inferred relationship Some 1
A rare hereditary ataxia with characteristics of adult onset of slowly progressive cerebellar degeneration with gait ataxia, dysmetria, dysarthria, and in some cases diplopia. Cognitive functions are normal, and seizures are absent. Magnetic resonance imaging reveals mild atrophy of the cerebellar vermis. Associated morphology True Degenerative abnormality Inferred relationship Some 1
A rare hereditary ataxia with characteristics of adult onset of slowly progressive cerebellar degeneration with gait ataxia, dysmetria, dysarthria, and in some cases diplopia. Cognitive functions are normal, and seizures are absent. Magnetic resonance imaging reveals mild atrophy of the cerebellar vermis. Associated morphology True Degenerative abnormality Inferred relationship Some 2
A rare genetic neurological syndrome of variable severity with characteristics of progressive spasticity affecting predominantly the lower limbs. Most patients manifest global developmental delay, moderate to severe intellectual disability and white matter abnormalities in infancy complicated by variable features including seizures, episodic respiratory failure, joint contractures and ocular problems. Some patients have normal early development until later childhood followed by regression in motor, cognitive and language skills over time. Some patients manifest only spastic paraplegia. Associated morphology True Degenerative abnormality Inferred relationship Some 1
Ab interno canaloplasty Procedure morphology (attribute) False Degenerative abnormality Inferred relationship Some 1
Osteoarthritis of bilateral subtalar joints (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 1
Osteoarthritis of bilateral subtalar joints (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 2
A rare genetic neurodegenerative disease with characteristics of childhood-onset severe developmental delay with regression, poor motor development, speech impairment and hypotonia due to CLCN6 mutations. Most of the patients have vision abnormalities, respiratory system abnormalities (including chronic respiratory insufficiency and tracheostomy that may lead to ventilator dependency) and feeding difficulties (percutaneous endoscopic gastronomy). Skin abnormalities including hyperhidrosis can be present. Associated morphology True Degenerative abnormality Inferred relationship Some 1
Left peripheral cystoid retinal degeneration Associated morphology True Degenerative abnormality Inferred relationship Some 1
Right peripheral cystoid retinal degeneration Associated morphology True Degenerative abnormality Inferred relationship Some 1
Posterior cord syndrome due to Friedreich ataxia (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 4
Posterior cord syndrome due to cervical spondylosis (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Elbow pain typically associated with overuse and degenerative change in enthesis of extensor carpi radialis brevis on lateral epicondyle of left humerus. Associated morphology True Degenerative abnormality Inferred relationship Some 1
Medial epicondylitis Associated morphology True Degenerative abnormality Inferred relationship Some 1
Lateral epicondylitis Associated morphology True Degenerative abnormality Inferred relationship Some 1
Elbow pain typically associated with overuse and degenerative change in enthesis of extensor carpi radialis brevis on lateral epicondyle of right humerus. Associated morphology True Degenerative abnormality Inferred relationship Some 1
Elbow pain typically associated with overuse and degenerative change in enthesis of extensor carpi radialis brevis on lateral epicondyle of both humeri. Associated morphology True Degenerative abnormality Inferred relationship Some 1
Elbow pain typically associated with overuse and degenerative change in enthesis of extensor carpi radialis brevis on lateral epicondyle of both humeri. Associated morphology True Degenerative abnormality Inferred relationship Some 2
Elbow pain typically associated with overuse and degenerative change in enthesis of extensor carpi radialis brevis on lateral epicondyle of humerus or of proximal common flexor tendon on medial epicondyle of humerus. Associated morphology True Degenerative abnormality Inferred relationship Some 1
Elbow pain typically associated with overuse and degenerative change in enthesis of proximal common flexor tendon on medial epicondyle of left humerus. Associated morphology True Degenerative abnormality Inferred relationship Some 1
Elbow pain typically associated with overuse and degenerative change in enthesis of proximal common flexor tendon on medial epicondyle of right humerus. Associated morphology True Degenerative abnormality Inferred relationship Some 1
Degeneration and inflammation (morphologic abnormality) Is a True Degenerative abnormality Inferred relationship Some
Degeneration of pupillary margin of left eye (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Right pupillary margin degeneration Associated morphology True Degenerative abnormality Inferred relationship Some 1
Bilateral pupillary margin degeneration Associated morphology True Degenerative abnormality Inferred relationship Some 1
Bilateral pupillary margin degeneration Associated morphology True Degenerative abnormality Inferred relationship Some 2
Prolapse of lumbar intervertebral disc co-occurrent and due to degeneration (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 3
Degeneration of seventh cervical intervertebral disc (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Diffuse cervicobrachial syndrome Associated morphology True Degenerative abnormality Inferred relationship Some 1
Kashin-Beck disease of joint of left wrist region (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Kashin-Beck disease of joint of wrist region (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Kashin-Beck disease of right wrist Associated morphology True Degenerative abnormality Inferred relationship Some 1
Kashin-Beck disease of joint of bilateral wrist regions (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Kashin-Beck disease of joint of bilateral wrist regions (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 2
Juvenile neuronal ceroid lipofuscinosis Associated morphology True Degenerative abnormality Inferred relationship Some 5
Arcus senilis Associated morphology True Degenerative abnormality Inferred relationship Some 2
Arcus juvenilis Associated morphology True Degenerative abnormality Inferred relationship Some 2
Congenital arcus juvenilis Associated morphology True Degenerative abnormality Inferred relationship Some 2
Bilateral arcus senilis Associated morphology True Degenerative abnormality Inferred relationship Some 1
A rare interstitial lung disease characterized by early-onset, severe, progressive lung disease manifesting by respiratory distress, neurological symptoms including axial hypotonia, developmental delay, irritability, dystonia, poor visual contact and seizures, and variable multisystemic involvement including malabsorption, progressive growth failure, recurrent infections, chronic hemolytic anemia and liver dysfunction. Kidney dysfunction, cardiac involvement including cardiomegaly and cardiac hypertrophy, decreased vision and strabismus have also been reported. Lung fibrosis may cause death in infancy from respiratory failure. Associated morphology True Degenerative abnormality Inferred relationship Some 1
A rare parkinsonian syndrome due to neurodegenerative disease characterised by resting tremor (which may initially be asymmetric), rigidity, and bradykinesia. Polyneuropathy with neurogenic electromyography findings is present in the majority of the patients and reported in young age (early twenties) whereas parkinsonian symptoms are visible later in life (between 40 and 70 years of age). Additional clinical symptoms may include anxiety and depression. Mild diffuse muscular atrophy can also be detected in some patients. Associated morphology True Degenerative abnormality Inferred relationship Some 1
A rare disorder of fatty acid biosynthesis characterised by spastic paraparesis, bilateral congenital/juvenile cataracts, gross motor developmental delay, speech delay and truncal hypotonia. Seizures in infancy can also be observed. Patients have elevated levels of ether lipids including plasmalogen. Majority of the affected individuals have normal brain imaging and normal growth. No microcephaly or dysmorphic features were reported. Associated morphology True Degenerative abnormality Inferred relationship Some 1

Start Previous Page 16 of 17 End

This concept is not in any reference sets

Back to Start