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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


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Degeneration Is a Degenerative abnormality false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Bilateral shoulder osteoarthritis Associated morphology False Degeneration Inferred relationship Some 2
    Sarcopenia Associated morphology False Degeneration Inferred relationship Some 1
    Autosomal recessive spastic paraplegia type 59 Associated morphology False Degeneration Inferred relationship Some 1
    Severe neurodegenerative syndrome with lipodystrophy Associated morphology False Degeneration Inferred relationship Some 2
    PRKAR1B-related neurodegenerative dementia with intermediate filaments Associated morphology False Degeneration Inferred relationship Some 1
    Ferro-cerebro-cutaneous syndrome Associated morphology False Degeneration Inferred relationship Some 1
    Fatal post-viral neurodegenerative disorder Associated morphology False Degeneration Inferred relationship Some 1
    Spondylosis of cervicothoracic spine Associated morphology False Degeneration Inferred relationship Some 1
    Spondylosis of cervicothoracic spine Associated morphology False Degeneration Inferred relationship Some 2
    Spondylosis of thoracolumbar spine (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Severe intellectual disability and progressive spastic paraplegia Associated morphology False Degeneration Inferred relationship Some 1
    Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Autosomal recessive spastic paraplegia type 27 Associated morphology False Degeneration Inferred relationship Some 1
    Primary non-essential cutis verticis gyrata (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Osteoarthritis of bilateral knee joints (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Osteoarthritis of bilateral knee joints (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Osteoarthritis of finger joint of right hand (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Osteoarthritis of joint of bilateral feet (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Osteoarthritis of joint of bilateral feet (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Osteoarthritis of joint of bilateral hands (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Osteoarthritis of joint of bilateral hands (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Osteoarthritis of finger joint of left hand (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Osteoarthritis of bilateral hip joints Associated morphology False Degeneration Inferred relationship Some 2
    Osteoarthritis of bilateral hip joints Associated morphology False Degeneration Inferred relationship Some 1
    Osteoarthritis of joint of finger of bilateral hands (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Osteoarthritis of joint of finger of bilateral hands (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Osteoarthritis of joint of bilateral ankles (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Osteoarthritis of joint of bilateral ankles (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Tendinosis of bilateral biceps brachii (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Tendinosis of bilateral biceps brachii (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Tendinosis of right knee (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Tendinosis of bilateral knees (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Tendinosis of bilateral knees (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Tendinosis of left knee (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Juvenile osteochondrosis of thoracic spine (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Juvenile osteochondrosis of thoracic spine (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Seropositive erosive rheumatoid arthritis (disorder) Associated morphology False Degeneration Inferred relationship Some 3
    Degenerative disorder of muscle Associated morphology False Degeneration Inferred relationship Some 2
    Autosomal recessive spastic paraplegia type 69 Associated morphology False Degeneration Inferred relationship Some 1
    Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Autosomal recessive spastic paraplegia type 60 Associated morphology False Degeneration Inferred relationship Some 1
    Autosomal recessive spastic paraplegia type 71 Associated morphology False Degeneration Inferred relationship Some 1
    Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Gemignani syndrome (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Autosomal spastic paraplegia type 72 Associated morphology False Degeneration Inferred relationship Some 1
    Autosomal recessive cerebellar ataxia due to STUB1 deficiency Associated morphology False Degeneration Inferred relationship Some 2
    Autosomal recessive cerebellar ataxia due to STUB1 deficiency Associated morphology False Degeneration Inferred relationship Some 1
    Autosomal dominant spastic paraplegia type 3 (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Infantile cerebellar and retinal degeneration (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Infantile cerebellar and retinal degeneration (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Circumferential viscodilation and tensioning of sinus venosus of sclera by external approach Procedure morphology (attribute) False Degeneration Inferred relationship Some 1
    Autosomal recessive spastic paraplegia type 14 Associated morphology False Degeneration Inferred relationship Some 1
    Progressive myoclonic epilepsy type 3 Associated morphology False Degeneration Inferred relationship Some 1
    Autosomal recessive cerebellar ataxia, psychomotor delay syndrome (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Autosomal recessive cerebellar ataxia, psychomotor delay syndrome (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Leigh syndrome with nephrotic syndrome Associated morphology False Degeneration Inferred relationship Some 1
    Infectious crystalline keratopathy Associated morphology False Degeneration Inferred relationship Some 2
    Autosomal dominant spastic paraplegia type 13 (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Autosomal recessive spastic paraplegia type 56 (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Age-related changes in ciliary body Associated morphology False Degeneration Inferred relationship Some 2
    Amyotrophic lateral sclerosis type 4 Associated morphology False Degeneration Inferred relationship Some 1
    Huntington disease-like 1 (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Adult-onset autosomal recessive cerebellar ataxia (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Adult-onset autosomal recessive cerebellar ataxia (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Thoracic spondylosis (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Thoracic spondylosis with radiculopathy Associated morphology False Degeneration Inferred relationship Some 2
    Single-level thoracic spondylosis with radiculopathy Associated morphology False Degeneration Inferred relationship Some 2
    Two-level thoracic spondylosis with radiculopathy Associated morphology False Degeneration Inferred relationship Some 2
    Multiple-level thoracic spondylosis with radiculopathy Associated morphology False Degeneration Inferred relationship Some 2
    Autosomal recessive spastic paraplegia type 24 Associated morphology False Degeneration Inferred relationship Some 1
    Autosomal dominant spastic paraplegia type 8 Associated morphology False Degeneration Inferred relationship Some 1
    Paving stone retinal degeneration of right eye (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Bilateral paving stone retinal degeneration Associated morphology False Degeneration Inferred relationship Some 1
    Bilateral paving stone retinal degeneration Associated morphology False Degeneration Inferred relationship Some 2
    Paving stone retinal degeneration of left eye (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Synucleinopathy Associated morphology False Degeneration Inferred relationship Some 1
    Pigmentary iris degeneration of bilateral eyes Associated morphology False Degeneration Inferred relationship Some 1
    Pigmentary iris degeneration of bilateral eyes Associated morphology False Degeneration Inferred relationship Some 2
    Bilateral arcus senilis Associated morphology False Degeneration Inferred relationship Some 1
    Dellen of cornea of right eye Associated morphology False Degeneration Inferred relationship Some 1
    Dellen of cornea of left eye (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Osteoarthritis of bilateral sternoclavicular joints (disorder) Associated morphology False Degeneration Inferred relationship Some 2
    Osteoarthritis of bilateral sternoclavicular joints (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Bilateral osteoarthritis of temporomandibular joints Associated morphology False Degeneration Inferred relationship Some 2
    Bilateral osteoarthritis of temporomandibular joints Associated morphology False Degeneration Inferred relationship Some 1
    Aneurysm osteoarthritis syndrome (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Ataxia with tapetoretinal degeneration syndrome Associated morphology False Degeneration Inferred relationship Some 2
    Hereditary sensory and autonomic neuropathy due to TECPR2 mutation Associated morphology False Degeneration Inferred relationship Some 1
    Single-level thoracic spondylosis with myelopathy Associated morphology False Degeneration Inferred relationship Some 3
    Autosomal recessive spastic paraplegia type 66 Associated morphology False Degeneration Inferred relationship Some 1
    Autosomal dominant spastic paraplegia type 38 (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Two-level thoracic spondylosis with myelopathy Associated morphology False Degeneration Inferred relationship Some 3
    Multiple-level thoracic spondylosis with myelopathy (disorder) Associated morphology False Degeneration Inferred relationship Some 3
    Vitreoretinal tuft of right eye Associated morphology False Degeneration Inferred relationship Some 2
    Vitreoretinal tuft of left eye Associated morphology False Degeneration Inferred relationship Some 2
    Brachydactyly, short stature, retinitis pigmentosa syndrome (disorder) Associated morphology False Degeneration Inferred relationship Some 3
    X-linked spastic paraplegia type 16 (disorder) Associated morphology False Degeneration Inferred relationship Some 1
    Bilateral arcus senilis Associated morphology False Degeneration Inferred relationship Some 2

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    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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