OMOP Concept 4047740
Bulbospinal neuronopathy
StandardConditionSNOMED230253001Disorder
Maps from
5
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
5 source codes normalize to Bulbospinal neuronopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 146849 | Bulbospinal Neuronopathy | Non-standard |
| MeSH | D055534 | Bulbo-Spinal Atrophy, X-Linked | Non-standard |
| Nebraska Lexicon | 10786008 | Spinobulbar atrophy | Non-standard |
| Nebraska Lexicon | 230253001 | Bulbospinal muscular atrophy | Non-standard |
| Read | F151300 | X-linked bulbo-spinal atrophy | Non-standard |
Synonyms
Alternative names recorded for Bulbospinal neuronopathy across source vocabularies.
- atrofia bulboespinal ligada al cromosoma X
- atrofia bulboespinal muscular
- Bulbospinal muscular atrophy
- Bulbospinal neuronopathy (disorder)
- Kennedy syndrome
- neuropatía bulboespinal
- neuropatía bulboespinal (trastorno)
- síndrome de Kennedy
- X-linked bulbospinal atrophy
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(17)Roll up to these when you need a wider cohort.
- 1Spinal muscular atrophy
- 1X-linked recessive hereditary disease
- 2Chronic nervous system disorder
- 2Hereditary motor neuron disease
- 2Lower motor neuron disease
- 2X-linked hereditary disease
- 3Chronic disease
- 3Disorder of nervous system
- 3Hereditary disorder of nervous system
- 3Motor neuron disease
- 3Sex-linked hereditary disorder
- 4Disease
- 4Disorder of body system
- 4Hereditary disease
- 4Hereditary disorder by system
- 5Clinical finding
- 5Genetic disease
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