OMOP Concept 4168666
Cerebral degeneration
StandardConditionSNOMED418143002Disorder
Maps from
9
Descendants
199
Valid from
31 Jan 2006
Valid to
31 Dec 2099
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Source codes that map to this concept
9 source codes normalize to Cerebral degeneration via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 119601 | Cerebral degeneration | Non-standard |
| HPO | HP_0007313 | Cerebral degeneration | Non-standard |
| ICD9CM | 331 | Other cerebral degenerations | Non-standard |
| ICD9CM | 331.8 | Other cerebral degeneration | Non-standard |
| ICD9CM | 331.89 | Other cerebral degeneration | Non-standard |
| ICD9CM | 331.9 | Cerebral degeneration, unspecified | Non-standard |
| Nebraska Lexicon | 418143002 | Cerebral degeneration | Non-standard |
| Read | F11yz00 | Other cerebral degeneration NOS | Non-standard |
| Read | F11z.00 | Cerebral degeneration NOS | Non-standard |
Synonyms
Alternative names recorded for Cerebral degeneration across source vocabularies.
- Cerebral degeneration (disorder)
- degeneración cerebral
- degeneración cerebral (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
- 1Degenerative brain disorder
- 2Degenerative disease of the central nervous system
- 2Disorder of brain
- 3Degenerative disorder
- 3Disorder of head
- 3Disorder of the central nervous system
- 3Finding of brain
- 4Central nervous system finding
- 4Disease
- 4Disorder of nervous system
- 4Head finding
- 5Clinical finding
- 5Disorder of body system
Narrower concepts
(199)Included automatically when you query with descendants.
- 1Atypical bovine spongiform encephalopathy
- 1Atypical scrapie Nor98
- 1Autosomal dominant striatal neurodegeneration
- 1Cerebral atrophy
- 1Cerebral calcification
- 1Cerebral degeneration associated with another disorder
- 1Cerebral degeneration in childhood
- 1Cerebral degeneration presenting primarily with dementia
- 1Chronic hepatocerebral degeneration
- 1Corticobasal degeneration
- 1Corticobasal syndrome
- 1Frontal lobe degeneration
- 1Frontotemporal degeneration
- 1Huntington disease-like 1
- 1Huntington disease-like 2
- 1Huntington disease-like syndrome due to C9ORF72 expansions
- 1Leukoencephalopathy with metaphyseal chondrodysplasia syndrome
- 1Neuroaxonal leukodystrophy
- 1Parkinsonism with polyneuropathy
- 1Parkinson's disease
- 1Pigmentary pallidal degeneration
- 1Pineal degeneration
- 1Pituitary degeneration
- 1Posterior cortical atrophy syndrome
- 1Progressive myoclonic epilepsy type 3
- 1Progressive supranuclear ophthalmoplegia
- 1Progressive supranuclear palsy
- 1Spongiform encephalopathy
- 1Striatonigral degeneration
- 1Vanishing white matter disease
- 1White matter disease
- 2Acquired cerebral atrophy
- 2Alzheimer's disease
- 2Argyrophilic grain disease
- 2Arteriopathic granular atrophy of cerebral cortex
- 2ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis
- 2Atrophy of corpus callosum
- 2Atypical bovine spongiform encephalopathy - H type
- 2Atypical bovine spongiform encephalopathy - L type
- 2Atypical pantothenate kinase associated neurodegeneration
- 2Atypical progressive supranuclear palsy syndrome
- 2Autosomal dominant late onset Parkinson disease
- 2Autosomal recessive cerebral atrophy
- 2Autosomal recessive familial Parkinson disease
- 2Bovine spongiform encephalopathy
- 2Calcification of basal ganglia
- 2Calcification of pineal gland
- 2Celiac disease with epilepsy and cerebral calcification syndrome
- 2Cerebral degeneration associated with generalized lipidosis
- 2Cerebral degeneration due to alcoholism
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