OMOP Concept 762970
Chronic myelopathy
StandardConditionSNOMED434371000124108Disorder
Maps from
1
Descendants
116
Valid from
1 Mar 2013
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Chronic myelopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 434371000124108 | Chronic spinal cord disorder | Non-standard |
Synonyms
Alternative names recorded for Chronic myelopathy across source vocabularies.
- Chronic disorder of spinal cord
- Chronic disorder of spinal cord (disorder)
- Chronic spinal cord disorder
- trastorno crónico de médula espinal
- trastorno crónico de médula espinal (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Chronic nervous system disorder
- 1Spinal cord disease
- 2Chronic disease
- 2Disorder of nervous system
- 2Disorder of spinal region
- 2Disorder of the central nervous system
- 2Finding of spinal cord
- 3Central nervous system finding
- 3Disease
- 3Disorder of back
- 3Disorder of body system
- 3Finding of spinal region
- 4Clinical finding
- 4Finding of back
Narrower concepts
(116)Included automatically when you query with descendants.
- 1Adult-onset autosomal recessive cerebellar ataxia
- 1ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis
- 1Autosomal recessive cerebellar ataxia, psychomotor delay syndrome
- 1Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
- 1Chronic venous infarction of spinal cord
- 1Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome
- 1Friedreich ataxia
- 1Hereditary spastic paraplegia
- 1Idiopathic feline polioencephalomyelitis
- 1Multiple sclerosis of the spinal cord
- 1Progressive congenital rubella encephalomyelitis
- 1PUM1-related cerebellar ataxia
- 1Spinocerebellar ataxia type 41
- 1Spinocerebellar ataxia type 42
- 1Spinocerebellar ataxia type 43
- 1Spinocerebellar ataxia type 45
- 1Spinocerebellar ataxia type 46
- 2Autosomal dominant hereditary spastic paraplegia
- 2Autosomal recessive hereditary spastic paraplegia
- 2Autosomal spastic paraplegia type 30
- 2Complicated hereditary spastic paraplegia
- 2Posterior cord syndrome due to Friedreich ataxia
- 2Posterior cord syndrome due to multiple sclerosis
- 2Pure hereditary spastic paraplegia
- 2X-linked hereditary spastic paraplegia
- 3Allan-Herndon-Dudley syndrome
- 3Autosomal dominant complex hereditary spastic paraplegia
- 3Autosomal dominant spastic paraplegia type 10
- 3Autosomal dominant spastic paraplegia type 12
- 3Autosomal dominant spastic paraplegia type 13
- 3Autosomal dominant spastic paraplegia type 19
- 3Autosomal dominant spastic paraplegia type 3
- 3Autosomal dominant spastic paraplegia type 31
- 3Autosomal dominant spastic paraplegia type 37
- 3Autosomal dominant spastic paraplegia type 4
- 3Autosomal dominant spastic paraplegia type 41
- 3Autosomal dominant spastic paraplegia type 42
- 3Autosomal dominant spastic paraplegia type 6
- 3Autosomal dominant spastic paraplegia type 73
- 3Autosomal dominant spastic paraplegia type 8
- 3Autosomal dominant spastic paraplegia type 9B
- 3Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction
- 3Autosomal recessive spastic paraplegia type 11
- 3Autosomal recessive spastic paraplegia type 14
- 3Autosomal recessive spastic paraplegia type 15
- 3Autosomal recessive spastic paraplegia type 18
- 3Autosomal recessive spastic paraplegia type 21
- 3Autosomal recessive spastic paraplegia type 23
- 3Autosomal recessive spastic paraplegia type 24
- 3Autosomal recessive spastic paraplegia type 25
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