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33359002: Degeneration (morphologic abnormality)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    55660014 Degeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    55662018 Degenerative change en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    764753012 Degeneration (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    55660014 Degeneration en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    55660014 Degeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    55662018 Degenerative change en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    55662018 Degenerative change en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    764753012 Degeneration (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    764753012 Degeneration (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    12461000077110 dégénérescence fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    12461000077110 dégénérescence fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    dégénérescence Is a Degenerative abnormality (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Lewy body dementia with behavioral disturbance (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 6
    Early onset Alzheimer's disease with behavioral disturbance Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Obliteration of root canal of tooth due to abnormal mineralization of tooth pulp (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Lichen sclerosus of penis (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 4
    Pingueculitis Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Primary osteoarthritis of ankle Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Secondary osteoarthritis of ankle (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Osteoarthritis of ankle secondary to trauma Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Primary calcaneocuboid osteoarthritis Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Osteoarthritis of calcaneocuboid joint (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Secondary calcaneocuboid osteoarthritis Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Calcaneocuboid osteoarthritis secondary to trauma Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Primary subtalar osteoarthritis Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Secondary osteoarthritis of subtalar joint Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Osteoarthritis of subtalar joint secondary to trauma (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Subtalar osteoarthritis secondary to inflammatory arthritis Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Osteoarthritis of calcaneocuboid joint secondary to inflammatory arthritis (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Osteoarthritis of ankle secondary to inflammatory arthritis (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Osteoarthritis of talonavicular joint Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Primary talonavicular osteoarthritis Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Secondary talonavicular osteoarthritis Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Talonavicular osteoarthritis secondary to trauma Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Talonavicular osteoarthritis secondary to inflammatory arthritis Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Secondary osteoarthritis of first metatarsophalangeal joint (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Primary osteoarthritis of first metatarsophalangeal joint Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Osteoarthritis of first metatarsophalangeal joint secondary to trauma Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Osteoarthritis of first metatarsophalangeal joint secondary to inflammatory arthritis (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital arcus juvenilis Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Amyloid pterygium Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 5
    Insertional Achilles tendinopathy (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Non-insertional Achilles tendinopathy (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Excision of pterygium with graft to conjunctiva (procedure) Procedure morphology (attribute) False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Excision of pterygium with graft to conjunctiva (procedure) Direct morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Excision of pterygium with amniotic membrane graft Procedure morphology (attribute) False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Excision of pterygium with amniotic membrane graft Direct morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Huntington disease-like syndrome Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    CHMP2B-related frontotemporal dementia Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    GRN-related frontotemporal dementia Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Aicardi's syndrome Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 4
    Aicardi's syndrome Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 5
    Congenital chorioretinal degeneration (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital chorioretinal degeneration (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Congenital degeneration of nervous system Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Aicardi's syndrome Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 6
    Congenital chorioretinal degeneration (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 4
    Macerated fetus Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Secondary osteoarthritis of midfoot Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Osteoarthritis of midfoot Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Primary osteoarthritis of midfoot (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Osteoarthritis of midfoot secondary to trauma Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Osteoarthritis of midfoot secondary to inflammatory arthritis Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Stickler syndrome Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 4
    Progressive epilepsy-intellectual disability syndrome Finnish type (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Infantile ascending hereditary spastic paralysis (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Retinal detachment and occipital encephalocele Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 6
    Spastic paraplegia type 15 Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Juvenile osteochondrosis of spine Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Degeneration of lumbosacral intervertebral disc Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hereditary hollow viscus myopathy Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital retinoschisis (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Iris and ciliary body degeneration Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Calve's vertebral osteochondrosis Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Infectious crystalline keratopathy Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Primary congenital glaucoma (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Juvenile retinoschisis Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Spinocerebellar ataxia type 36 (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Spinocerebellar ataxia type 36 (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Thoracic spondylosis with myelopathy Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 5
    Single-level thoracic spondylosis with myelopathy Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 5
    Two-level thoracic spondylosis with myelopathy (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 5
    Multiple-level thoracic spondylosis with myelopathy Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 5
    Osteoarthritis of hip due to dysplasia (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Cerebral degeneration due to hypothyroidism Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Cerebral degeneration due to alcoholism (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Degenerative brain disorder caused by alcohol Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Osteoarthritis of facet joint of thoracic spine (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Osteoarthritis of lumbar spinal facet joint Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Sporadic Creutzfeldt-Jakob disease Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Cerebral degeneration due to progressive multifocal leukoencephalopathy Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Cochleosaccular degeneration and cataract syndrome (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Spastic paraplegia type 7 (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    A complex hereditary spastic paraplegia characterised by progressive lower limbs weakness and spasticity, upper limbs weakness, dysarthria, hypomimia, sphincter disturbances, peripheral neuropathy, learning difficulties, cognitive impairment and dementia. Magnetic resonance imaging shows thin corpus callosum, cerebral atrophy, and periventricular white matter changes. Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Spastic paraparesis and deafness Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 6
    Spinocerebellar ataxia type 7 (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Spinocerebellar ataxia type 7 (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Spinocerebellar ataxia type 1 (SCA1) is a subtype of type I autosomal dominant cerebellar ataxia characterised by dysarthria, writing difficulties, limb ataxia, and commonly nystagmus and saccadic abnormalities. Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Spinocerebellar ataxia type 1 (SCA1) is a subtype of type I autosomal dominant cerebellar ataxia characterised by dysarthria, writing difficulties, limb ataxia, and commonly nystagmus and saccadic abnormalities. Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Spinocerebellar ataxia type 2 (SCA2) is a subtype of type I autosomal dominant cerebellar ataxia characterised by truncal ataxia, dysarthria, slowed saccades and less commonly ophthalmoparesis and chorea. Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Spinocerebellar ataxia type 2 (SCA2) is a subtype of type I autosomal dominant cerebellar ataxia characterised by truncal ataxia, dysarthria, slowed saccades and less commonly ophthalmoparesis and chorea. Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Spinocerebellar ataxia type 6 (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Spinocerebellar ataxia type 6 (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Spinocerebellar ataxia type 8 (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Spinocerebellar ataxia type 8 (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Spinocerebellar ataxia type 10 (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Spinocerebellar ataxia type 10 (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia characterized by ataxia with sensory neuropathy. Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia characterized by ataxia with sensory neuropathy. Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Richards-Rundle syndrome (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Richards-Rundle syndrome (disorder) Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 4
    A rare autosomal recessive cerebellar ataxia characterized by early onset of non- or slowly progressive cerebellar signs and symptoms including truncal and gait ataxia, dysarthria, dysmetria, dysdiadochokinesis, tremor, and nystagmus. Delayed psychomotor development and intellectual disability are variable. Additional reported features are spasticity, hypotonia, cataracts, and sensorineural hearing loss, among others. Brain imaging shows cerebellar atrophy. Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 3
    A rare autosomal recessive cerebellar ataxia characterized by early onset of non- or slowly progressive cerebellar signs and symptoms including truncal and gait ataxia, dysarthria, dysmetria, dysdiadochokinesis, tremor, and nystagmus. Delayed psychomotor development and intellectual disability are variable. Additional reported features are spasticity, hypotonia, cataracts, and sensorineural hearing loss, among others. Brain imaging shows cerebellar atrophy. Associated morphology False dégénérescence Inferred relationship Existential restriction modifier (core metadata concept) 5

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    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    SAME AS association reference set (foundation metadata concept)

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