OMOP Concept 37116352
Autosomal dominant spastic paraplegia type 29
StandardConditionSNOMED733029008Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal dominant spastic paraplegia type 29 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536863 | Spastic paraplegia 29, autosomal dominant | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant spastic paraplegia type 29 across source vocabularies.
- Autosomal dominant spastic paraplegia type 29 (disorder)
- paraplejía espástica autosómica dominante tipo 29
- paraplejía espástica autosómica dominante tipo 29 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(58)Roll up to these when you need a wider cohort.
- 1Autosomal dominant complex hereditary spastic paraplegia
- 1Decreased hearing
- 1Hereditary hearing loss
- 1Sensorineural hearing loss
- 2Auditory system hereditary disorder
- 2Autosomal dominant hereditary spastic paraplegia
- 2Complicated hereditary spastic paraplegia
- 2Decline in functional status
- 2Hearing finding
- 2Hearing loss
- 3Autosomal dominant hereditary disorder
- 3Disorder of auditory system
- 3Ear and auditory finding
- 3Functional finding
- 3Hearing disorder
- 3Hereditary disorder by system
- 3Hereditary spastic paraplegia
- 4Autosomal hereditary disorder
- 4Chronic myelopathy
- 4Chronic paraplegia
- 4Clinical finding
- 4Disorder of body system
- 4Hereditary degenerative disease of central nervous system
- 4Hereditary disease
- 4Spastic paraplegia
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