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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
Progressive epilepsy-intellectual disability syndrome Finnish type Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Retinal detachment and occipital encephalocele Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Infantile ascending hereditary spastic paralysis Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Retinoschisis Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Juvenile cerebellar degeneration AND myoclonus Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Degeneration of intervertebral disc Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Nodular degeneration of cornea Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Nutritional muscular degeneration Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Hereditary choroidal dystrophy Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Primary localized osteoarthrosis of pelvic region Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Interphalangeal osteoarthritis Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Juvenile osteochondrosis of symphysis pubis Associated morphology False Degenerative abnormality Inferred relationship Existential restriction modifier 2
Choroideremia with deafness and obesity syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 26 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 26 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 25 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 25 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 20 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 20 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 23 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 23 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 21 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 21 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
X-linked neurodegenerative syndrome Hamel type Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
X-linked neurodegenerative syndrome Bertini type Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 39 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 11 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 11 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 12 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 12 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 13 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 13 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 14 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 14 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 17 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 17 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 18 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 18 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 19 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 19 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 27 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 27 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 30 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 30 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 32 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 32 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 34 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 4
Spinocerebellar ataxia type 34 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 3
Spinocerebellar ataxia type 35 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 35 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 37 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 37 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 5 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 5 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
X-linked sideroblastic anemia with spinocerebellar ataxia Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
X-linked sideroblastic anemia with spinocerebellar ataxia Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 5
X-linked spinocerebellar ataxia type 3 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
X-linked spinocerebellar ataxia type 3 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
X-linked spinocerebellar ataxia type 4 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
X-linked spinocerebellar ataxia type 4 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 3
Spinocerebellar degeneration and corneal dystrophy syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar degeneration and corneal dystrophy syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Neuronal ceroid lipofuscinosis due to deficiency of cathepsin D Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Non-amnestic Alzheimer disease Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Adult retinoschisis Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Primary progressive apraxia of speech Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Choroideremia Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Facial onset sensory and motor neuronopathy syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Hypotrichosis with juvenile macular degeneration syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
X-linked spastic paraplegia type 2 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 36 Associated morphology False Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 4 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 44 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 46 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 53 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 54 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 55 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 57 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Retinohepatoendocrinologic syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Tendinosis Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Infantile onset spinocerebellar ataxia Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Infantile onset spinocerebellar ataxia Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Intervertebral disc degeneration of cervical spine without prolapsed disc Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Chorea co-occurrent and due to Wilson disease Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 5
Chorea co-occurrent and due to Wilson disease Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Chorea co-occurrent and due to Wilson disease Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
X-linked hereditary spastic paraplegia Associated morphology False Degenerative abnormality Inferred relationship Existential restriction modifier 2
Autonomic nervous system disorder co-occurrent and due to neurodegenerative disorder Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 3
Epilepsy co-occurrent and due to degenerative brain disorder Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spastic paraplegia, optic atrophy, neuropathy syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal dominant striatal neurodegeneration Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Familial Scheuermann disease Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 32 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 26 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 23 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 64 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 63 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 61 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spastic paraplegia with Paget disease of bone syndrome Associated morphology False Degenerative abnormality Inferred relationship Existential restriction modifier 1

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