OMOP Concept 37472266
Autosomal dominant spastic paraplegia type 79A
StandardConditionSNOMED1375927000Disorder
Maps from
0
Descendants
0
Valid from
1 Oct 2025
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Autosomal dominant spastic paraplegia type 79A across source vocabularies.
- Autosomal dominant spastic paraplegia 79A with ataxia
- Autosomal dominant spastic paraplegia type 79A (disorder)
- paraplejía espástica autosómica dominante 79A con ataxia
- paraplejía espástica autosómica dominante tipo 79A
- paraplejía espástica autosómica dominante tipo 79A (trastorno)
- paraplejía espástica autosómica dominante tipo 79 relacionada con gen UCHL1
- SPG79A - paraplejía espástica tipo 79A
- SPG79A - spastic paraplegia type 79A
- UCHL1-gene related autosomal dominant spastic paraplegia type 79
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(49)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary spastic paraplegia
- 1Bilateral lower limb ataxia
- 1Hereditary ataxia
- 2Ataxia
- 2Autosomal dominant hereditary disorder
- 2Finding of lower limb
- 2Hereditary disorder of nervous system
- 2Hereditary spastic paraplegia
- 3Autosomal hereditary disorder
- 3Chronic myelopathy
- 3Chronic paraplegia
- 3Disorder of nervous system
- 3Finding of limb structure
- 3Finding related to coordination / incoordination
- 3Hereditary degenerative disease of central nervous system
- 3Hereditary disorder by system
- 3Spastic paraplegia
- 4Chronic nervous system disorder
- 4Clinical finding
- 4Degenerative disease of the central nervous system
- 4Disorder of body system
- 4Hereditary disease
- 4Paraplegia
- 4Spastic syndrome
- 4Spinal cord disease
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