autosomal dominant Spastic paraplegia 3

Hereditary autosomal dominant spastic paraplegia that is associated with mutations in the ATL1 gene. OMIM: 182600

Also Known As:

Spastic paraplegia 3, autosomal dominant; Familial spastic paraplegia, autosomal dominant, 1; Fsp1 Familial spastic paraplegia 1; SPG3A Spastic paraplegia 3a; Spastic Paraplegia 3; Spastic Paraplegia 3a; Spastic Paraplegia Type 3a; Spg3a; Strumpell disease

Nervous System Diseases: 14737
- Neurodegenerative Diseases: 44095
  - Nervous System Heredodegenerative Disorders: 62
    - Hereditary Sensory and Motor Neuropathy: 260
      - Hereditary Spastic Paraplegia: 542
        autosomal dominant Spastic paraplegia 3: 45
- Neuromuscular Diseases: 2048
  - Peripheral Nervous System Diseases: 11768
    - Polyneuropathies: 5219
      - Hereditary Sensory and Motor Neuropathy: 260
        Hereditary Spastic Paraplegia: 542
        autosomal dominant Spastic paraplegia 3: 45
- Nervous System Malformations: 36
  - Hereditary Sensory and Motor Neuropathy: 260
    - Hereditary Spastic Paraplegia: 542
      - autosomal dominant Spastic paraplegia 3: 45
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Congenital Abnormalities: 26404
  - Nervous System Malformations: 36
    - Hereditary Sensory and Motor Neuropathy: 260
      - Hereditary Spastic Paraplegia: 542
        autosomal dominant Spastic paraplegia 3: 45
- Inborn Genetic Diseases: 12342
  - Nervous System Heredodegenerative Disorders: 62
    - Hereditary Sensory and Motor Neuropathy: 260
      - Hereditary Spastic Paraplegia: 542
        autosomal dominant Spastic paraplegia 3: 45

M Latouche Selected Research

M Latouche Research Topics

Disease

Drug/Important Bio-Agent (IBA)