OMOP Concept 35622060
Autosomal dominant spastic paraplegia type 19
StandardConditionSNOMED763375003Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2018
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 19 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536856 | Spastic paraplegia 19, autosomal dominant | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant spastic paraplegia type 19 across source vocabularies.
- Autosomal dominant spastic paraplegia type 19 (disorder)
- paraplejía espástica autosómica dominante tipo 19
- paraplejía espástica autosómica dominante tipo 19 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(46)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary spastic paraplegia
- 1Pure hereditary spastic paraplegia
- 2Autosomal dominant hereditary disorder
- 2Hereditary spastic paraplegia
- 3Autosomal hereditary disorder
- 3Chronic myelopathy
- 3Chronic paraplegia
- 3Hereditary degenerative disease of central nervous system
- 3Spastic paraplegia
- 4Chronic nervous system disorder
- 4Degenerative disease of the central nervous system
- 4Hereditary disease
- 4Hereditary disorder of nervous system
- 4Paraplegia
- 4Spastic syndrome
- 4Spinal cord disease
- 5Bilateral lower limb paralytic syndrome
- 5Chronic disease
- 5Complete bilateral paralysis
- 5Degenerative disorder
- 5Disorder of nervous system
- 5Disorder of spinal region
- 5Disorder of the central nervous system
- 5Finding of spinal cord
- 5Genetic disease
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