Spinocerebellar ataxia 14

A hereditary autosomal dominant spinocerebellar ataxia with a mean age of onset of 31 years. It is characterized primarily by GAIT ATAXIA; cerebellar DYSARTHRIA, slowed SACCADES, ocular dysmetria, and HYPERREFLEXIA. Mutations in the PRKCG gene have been identified. OMIM: 605361

Also Known As:

SCA14 Spinocerebellar ataxia 14

Nervous System Diseases: 14737
- Neurodegenerative Diseases: 44095
  - Nervous System Heredodegenerative Disorders: 62
    - Spinocerebellar Degenerations: 355
      - Spinocerebellar Ataxias: 2124
        Spinocerebellar ataxia 14: 8
- Neurologic Manifestations: 7223
  - Dyskinesias: 7933
    - Ataxia: 6487
      - Cerebellar Ataxia: 1566
        Spinocerebellar Ataxias: 2124
        Spinocerebellar ataxia 14: 8
- Central Nervous System Diseases: 4371
  - Brain Diseases: 16141
    - Cerebellar Diseases: 647
      - Cerebellar Ataxia: 1566
        Spinocerebellar Ataxias: 2124
        Spinocerebellar ataxia 14: 8
      - Spinocerebellar Degenerations: 355
        Spinocerebellar Ataxias: 2124
        Spinocerebellar ataxia 14: 8
  - Spinal Cord Diseases: 4420
    - Spinocerebellar Degenerations: 355
      - Spinocerebellar Ataxias: 2124
        Spinocerebellar ataxia 14: 8
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Nervous System Heredodegenerative Disorders: 62
    - Spinocerebellar Degenerations: 355
      - Spinocerebellar Ataxias: 2124
        Spinocerebellar ataxia 14: 8

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