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107669003: Degenerative abnormality (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
172105010 Degenerative abnormality en Synonym Active Entire term case insensitive SNOMED CT core module
593391011 Degenerative abnormality (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module

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

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