OMOP Concept 4213310
Degenerative disease of the central nervous system
StandardConditionSNOMED80690008Disorder
Maps from
37
Descendants
702
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
37 source codes normalize to Degenerative disease of the central nervous system via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Degenerative disease of the central nervous system across source vocabularies.
- Degenerative disease of the central nervous system (disorder)
- enfermedad degenerativa del sistema nervioso central
- enfermedad degenerativa del sistema nervioso central (trastorno)
- enfermedad degenerativa del SNC
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(7)Roll up to these when you need a wider cohort.
Narrower concepts
(702)Included automatically when you query with descendants.
- 1Amyotrophic lateral sclerosis, parkinsonism, dementia complex
- 1Autonomic nervous system disorder co-occurrent and due to neurodegenerative disorder
- 1Bovine progressive degenerative myeloencephalopathy
- 1Central nervous system calcification, deafness, tubular acidosis, anemia syndrome
- 1Congenital ischemic atrophy of central nervous system structure
- 1Degenerative brain disorder
- 1Degenerative myelopathy
- 1Demyelinating disease of central nervous system
- 1Documentation stating patient has a diagnosis of a degenerative neurological condition such as als, ms, or parkinson's diagnosed at any time before or during the episode of care
- 1Hereditary degenerative disease of central nervous system
- 1Idiopathic feline polioencephalomyelitis
- 1Leukodystrophy
- 1Optic atrophy
- 1Optic nerve and photoreceptor degeneration
- 1Ossifying pachymeningitis
- 1Spinal ataxia
- 1Subacute combined degeneration of spinal cord
- 1Synucleinopathy
- 24H leukodystrophy
- 2Acute disseminated encephalomyelitis
- 2Adrenoleukodystrophy
- 2Adult onset autosomal dominant leukodystrophy
- 2Aicardi Goutieres syndrome
- 2Alexander disease
- 2Alkaline ceramidase 3 deficiency
- 2Amyotrophic lateral sclerosis type 4
- 2Arrested hydrocephalus
- 2Atrophy of optic disc
- 2Atypical Krabbe disease due to saposin A deficiency
- 2Atypical pantothenate kinase associated neurodegeneration
- 2Auditory neuropathy, optic atrophy syndrome
- 2Autonomic disorder due to multiple sclerosis
- 2Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein
- 2Autosomal dominant Alzheimer disease due to mutation of presenilin 1
- 2Autosomal dominant Alzheimer disease due to mutation of presenilin 2
- 2Autosomal dominant late onset basal ganglia degeneration
- 2Autosomal dominant late onset Parkinson disease
- 2Autosomal dominant striatal neurodegeneration
- 2Autosomal recessive cerebral atrophy
- 2Autosomal recessive familial Parkinson disease
- 2Autosomal recessive isolated optic atrophy
- 2Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome
- 2Balo concentric sclerosis
- 2Behavioral variant of frontotemporal dementia
- 2Brain calcification Rajab type
- 2C11ORF73-related autosomal recessive hypomyelinating leukodystrophy
- 2CAMOS syndrome
- 2Cavitating leukodystrophy
- 2Central nervous system demyelination due to Lyme borreliosis
- 2Central nervous system demyelination due to Whipple disease
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