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Autosomal Dominant Spastic Paraplegia 33

also known as SPG33; associated with mutations in ZFYVE27, the gene for zinc finger FYVE domain-containing protein 27

Also Known As:

Spastic Paraplegia 33, Autosomal Dominant

Networked: 0 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Nervous System Diseases: 14178
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Nervous System Malformations: 35
    - Hereditary Sensory and Motor Neuropathy: 249
      - Hereditary Spastic Paraplegia: 528
        Autosomal Dominant Spastic Paraplegia 33
- Inborn Genetic Diseases: 11939
  - Nervous System Heredodegenerative Disorders: 63
    - Hereditary Sensory and Motor Neuropathy: 249
      - Hereditary Spastic Paraplegia: 528
        Autosomal Dominant Spastic Paraplegia 33