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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

194 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Degenerative abnormality Is a Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Osteoarthritis of bilateral hip joints due to and following trauma (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 4
Osteoarthritis of bilateral hip joints due to and following trauma (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 2
Westphal-Strumpell syndrome Associated morphology True Degenerative abnormality Inferred relationship Some 1
Westphal-Strumpell syndrome Associated morphology True Degenerative abnormality Inferred relationship Some 2
Westphal-Strumpell syndrome Associated morphology True Degenerative abnormality Inferred relationship Some 3
X-linked complex hereditary spastic paraplegia Associated morphology False Degenerative abnormality Inferred relationship Some 2
X-linked pure hereditary spastic paraplegia Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal recessive familial Parkinson disease Associated morphology True Degenerative abnormality Inferred relationship Some 1
Juvenile osteochondrosis of tarsus (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal dominant Alzheimer disease due to mutation of presenilin 2 (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal dominant Alzheimer disease due to mutation of presenilin 1 (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein Associated morphology True Degenerative abnormality Inferred relationship Some 1
Atypical progressive supranuclear palsy syndrome Associated morphology True Degenerative abnormality Inferred relationship Some 1
Progressive supranuclear palsy parkinsonism syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Progressive supranuclear palsy progressive non fluent aphasia Associated morphology True Degenerative abnormality Inferred relationship Some 1
Progressive supranuclear palsy corticobasal syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 2
Felty syndrome with seronegative erosive rheumatoid arthritis (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Degenerating leiomyoma Is a False Degenerative abnormality Inferred relationship Some
Anti-citrullinated protein antibody positive erosive rheumatoid arthritis Associated morphology True Degenerative abnormality Inferred relationship Some 1
Rheumatoid factor and anti-citrullinated protein antibody positive erosive rheumatoid arthritis Associated morphology True Degenerative abnormality Inferred relationship Some 1
Seronegative erosive rheumatoid arthritis Associated morphology True Degenerative abnormality Inferred relationship Some 1
Oligoarticular osteoarthritis Associated morphology False Degenerative abnormality Inferred relationship Some 1
Psychosis co-occurrent and due to Parkinson's disease (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 3
Degenerative sequelae of disorders Associated morphology True Degenerative abnormality Inferred relationship Some 2
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder Associated morphology True Degenerative abnormality Inferred relationship Some 1
Childhood-onset basal ganglia degeneration syndrome Associated morphology True Degenerative abnormality Inferred relationship Some 1
Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 76 (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 2
Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 2
Menkes kinky-hair syndrome Associated morphology True Degenerative abnormality Inferred relationship Some 2
Allan-Herndon-Dudley syndrome Associated morphology True Degenerative abnormality Inferred relationship Some 1
Severe X-linked mitochondrial encephalomyopathy (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 3
X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Acyl-CoA oxidase deficiency Associated morphology True Degenerative abnormality Inferred relationship Some 1
Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome Associated morphology True Degenerative abnormality Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 78 (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Degeneration of uterine fibroid Associated morphology True Degenerative abnormality Inferred relationship Some 1
Deep sclerectomy without spacer (procedure) Procedure morphology (attribute) False Degenerative abnormality Inferred relationship Some 2
Deep sclerectomy with spacer (procedure) Procedure morphology (attribute) False Degenerative abnormality Inferred relationship Some 2
Deep sclerectomy (procedure) Procedure morphology (attribute) False Degenerative abnormality Inferred relationship Some 3
Deep sclerectomy with collagen implant (procedure) Procedure morphology (attribute) False Degenerative abnormality Inferred relationship Some 3
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder) Associated morphology False Degenerative abnormality Inferred relationship Some 2
Spinocerebellar ataxia due to vitamin E deficiency (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Spinocerebellar ataxia due to vitamin E deficiency (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 2
Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 74 Associated morphology True Degenerative abnormality Inferred relationship Some 3
Spastic paraplegia, severe developmental delay, epilepsy syndrome Associated morphology True Degenerative abnormality Inferred relationship Some 4
Autosomal dominant hereditary spastic paraplegia Associated morphology True Degenerative abnormality Inferred relationship Some 3
X-linked hereditary spastic paraplegia (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal recessive hereditary spastic paraplegia Associated morphology True Degenerative abnormality Inferred relationship Some 1
Pure hereditary spastic paraplegia Associated morphology True Degenerative abnormality Inferred relationship Some 3
Complicated hereditary spastic paraplegia Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal spastic paraplegia type 30 (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 35 Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 62 Associated morphology True Degenerative abnormality Inferred relationship Some 1
Hereditary spastic paraplegia Associated morphology True Degenerative abnormality Inferred relationship Some 3
Hereditary sensory and autonomic neuropathy with spastic paraplegia (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 36 (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 3
Spastic paraplegia with Paget disease of bone syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 4
Spastic paraplegia with precocious puberty syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 29 (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 3
Spastic paraplegia, nephritis, deafness syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 3
X-linked complex hereditary spastic paraplegia Associated morphology True Degenerative abnormality Inferred relationship Some 1
Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 12 (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 19 Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 28 Associated morphology True Degenerative abnormality Inferred relationship Some 1
Spastic paraplegia, facial cutaneous lesion syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 31 (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 42 Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 37 (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Intellectual disability, spasticity, ectrodactyly syndrome Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 9A Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 9B Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 9B Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 73 Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 75 (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 77 Associated morphology True Degenerative abnormality Inferred relationship Some 1
Pituitary degeneration Associated morphology True Degenerative abnormality Inferred relationship Some 1
Leigh syndrome due to cytochrome C oxidase deficiency (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 2
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 2
Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus Associated morphology True Degenerative abnormality Inferred relationship Some 2
Autosomal dominant amyotrophic lateral sclerosis type 1 Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal recessive amyotrophic lateral sclerosis type 1 Associated morphology True Degenerative abnormality Inferred relationship Some 1
Amyotrophic lateral sclerosis type 1 Associated morphology True Degenerative abnormality Inferred relationship Some 1
Fibrocystic renal degeneration Associated morphology True Degenerative abnormality Inferred relationship Some 1
Amyotrophic lateral sclerosis type 6 Associated morphology True Degenerative abnormality Inferred relationship Some 1
Amyotrophic lateral sclerosis type 3 Associated morphology True Degenerative abnormality Inferred relationship Some 2
Amyotrophic lateral sclerosis type 7 (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Amyotrophic lateral sclerosis type 8 Associated morphology True Degenerative abnormality Inferred relationship Some 1
Amyotrophic lateral sclerosis type 9 (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 2
Severe oculo-renal-cerebellar syndrome (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 2
Amyotrophic lateral sclerosis type 10 (disorder) Associated morphology True Degenerative abnormality Inferred relationship Some 1
Familial infantile bilateral striatal necrosis Associated morphology True Degenerative abnormality Inferred relationship Some 1
Spinocerebellar ataxia type 41 Associated morphology True Degenerative abnormality Inferred relationship Some 1
Spinocerebellar ataxia type 41 Associated morphology True Degenerative abnormality Inferred relationship Some 2

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