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33359002: Degeneration (morphologic abnormality)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    55660014 Degeneration en Synonym Active Entire term case insensitive SNOMED CT core module
    55662018 Degenerative change en Synonym Active Entire term case insensitive SNOMED CT core module
    764753012 Degeneration (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Degeneration Is a Degenerative abnormality false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Tendinosis of bilateral shoulders Associated morphology False Degeneration Inferred relationship Existential restriction modifier 3
    Tendinosis of bilateral shoulders Associated morphology False Degeneration Inferred relationship Existential restriction modifier 4
    Acquired hypoganglionosis of large intestine Associated morphology False Degeneration Inferred relationship Existential restriction modifier 3
    Acquired hypoganglionosis of large intestine Associated morphology False Degeneration Inferred relationship Existential restriction modifier 4
    Autosomal dominant hereditary spastic paraplegia Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Subconjunctival degeneration Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Degeneration of posterior pole of eye Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Miner's knee Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Tendinosis of right knee Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Tendinosis of left knee Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Degeneration of spine Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Lipodermatosclerosis of lower limb due to varicose veins of lower limb Associated morphology False Degeneration Inferred relationship Existential restriction modifier 12
    Autosomal dominant spastic paraplegia type 31 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Autosomal spastic paraplegia type 30 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Spastic paraplegia, facial cutaneous lesion syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Actinic cheilitis Associated morphology False Degeneration Inferred relationship Existential restriction modifier 3
    Osteoarthritis of midtarsal joints of bilateral feet Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Autosomal recessive spastic paraplegia type 35 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Autosomal recessive spastic paraplegia type 62 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Spinocerebellar ataxia with axonal neuropathy type 1 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Autosomal recessive spastic paraplegia type 43 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Spinocerebellar ataxia with axonal neuropathy type 1 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Autosomal recessive spastic paraplegia type 5A Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Autosomal recessive spastic paraplegia type 21 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Osteoarthritis of midtarsal joints of bilateral feet Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Autosomal dominant spastic paraplegia type 19 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Spastic paraplegia, neuropathy, poikiloderma syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    X-linked spastic paraplegia type 34 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Primary essential cutis verticis gyrata Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Autosomal recessive spastic paraplegia type 15 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Autosomal recessive spastic paraplegia type 48 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Autosomal dominant spastic paraplegia type 41 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Autosomal dominant spastic paraplegia type 42 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Autosomal dominant spastic paraplegia type 12 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Hypotonia, speech impairment, severe cognitive delay syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Autosomal recessive spastic paraplegia type 28 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Autosomal dominant spastic paraplegia type 37 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Degenerative rupture of lateral meniscus of bilateral knees Associated morphology False Degeneration Inferred relationship Existential restriction modifier 4
    Degenerative rupture of lateral meniscus of bilateral knees Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Autosomal recessive spastic paraplegia type 45 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Autosomal recessive spastic paraplegia type 67 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Mixed dementia Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Acquired hypoganglionosis of large intestine Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Acquired hypoganglionosis of large intestine Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Hereditary hollow viscus myopathy Associated morphology False Degeneration Inferred relationship Existential restriction modifier 3
    Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Autosomal dominant spastic paraplegia type 17 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Band keratopathy of right eye Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Band keratopathy of bilateral eyes Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Band keratopathy of bilateral eyes Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Band keratopathy of left eye Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Degenerative progressive high myopia of bilateral eyes Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Degenerative progressive high myopia of bilateral eyes Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Degenerative progressive high myopia of left eye Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Nodular degeneration of bilateral corneas Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Nodular degeneration of bilateral corneas Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Nodular degeneration of left cornea Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Myopic macular degeneration of left eye Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Myopic macular degeneration of right eye Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Degenerative progressive high myopia of right eye Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Nodular degeneration of right cornea Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Autosomal recessive spastic paraplegia type 58 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Autosomal recessive spastic paraplegia type 70 Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Pinguecula of bilateral eyes Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Autosomal dominant neovascular inflammatory vitreoretinopathy Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Pinguecula of left eye Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Vitreous degeneration of right eye Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Vitreous degeneration of left eye Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Vitreous degeneration of bilateral eyes Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Vitreous degeneration of bilateral eyes Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Lattice degeneration of right retina Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Lattice degeneration of right retina Associated morphology False Degeneration Inferred relationship Existential restriction modifier 3
    Lattice degeneration of left retina Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Lattice degeneration of left retina Associated morphology False Degeneration Inferred relationship Existential restriction modifier 3
    Lattice degeneration of bilateral retinas Associated morphology False Degeneration Inferred relationship Existential restriction modifier 3
    Lattice degeneration of bilateral retinas Associated morphology False Degeneration Inferred relationship Existential restriction modifier 4
    Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Schisis of right retina Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Schisis of left retina Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Retinoschisis and retinal cysts Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Schisis of bilateral retinas Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Flat retinoschisis Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Aicardi's syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 3
    Congenital degeneration of nervous system Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Schisis of bilateral retinas Associated morphology False Degeneration Inferred relationship Existential restriction modifier 3
    Spinocerebellar ataxia dysmorphism syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 3
    Spinocerebellar ataxia dysmorphism syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 4
    Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Congenital chorioretinal degeneration Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Encephalopathy, intracerebral calcification, retinal degeneration syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Hypotrichosis with juvenile macular degeneration syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 3
    Van den Bosch syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Stickler syndrome Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Osteoarthritis of bilateral wrists Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Osteoarthritis of bilateral wrists Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2
    Osteoarthritis of bilateral shoulders Associated morphology False Degeneration Inferred relationship Existential restriction modifier 1
    Osteoarthritis of bilateral shoulders Associated morphology False Degeneration Inferred relationship Existential restriction modifier 2

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