X-Linked Bulbo-Spinal Atrophy

An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR.

Also Known As:

Bulbo-Spinal Atrophy, X-Linked; Bulbospinal Muscular Atrophy, X-linked; Kennedy Disease; Kennedy Spinal and Bulbar Muscular Atrophy; Kennedy's Disease; Spinal And Bulbar Muscular Atrophy, X-Linked 1; Spinal and Bulbar Muscular Atrophy; X-Linked Spinal and Bulbar Muscular Atrophy; X-linked Bulbospinal Muscular Atrophy; Atrophies, X-Linked Bulbo-Spinal; Atrophy, Spinobulbar Muscular; Atrophy, X-Linked Bulbo-Spinal; Bulbo Spinal Atrophy, X Linked; Bulbo-Spinal Atrophies, X-Linked; Bulbospinal Muscular Atrophy, X linked; Spinal And Bulbar Muscular Atrophy, X Linked 1; Spinobulbar Muscular Atrophies; X Linked Bulbo Spinal Atrophy; X Linked Spinal and Bulbar Muscular Atrophy; X linked Bulbospinal Muscular Atrophy; X-Linked Bulbo-Spinal Atrophies; Atrophy, Muscular, Spinobulbar; Kennedy Syndrome; Muscular Atrophy, Spinobulbar; Spinobulbar Muscular Atrophy

Nervous System Diseases: 14737
- Neurodegenerative Diseases: 44095
  - Motor Neuron Disease: 1851
    - Spinal Muscular Atrophy: 2346
      - X-Linked Bulbo-Spinal Atrophy: 548
  - Nervous System Heredodegenerative Disorders: 62
    - X-Linked Bulbo-Spinal Atrophy: 548
- Central Nervous System Diseases: 4371
  - Spinal Cord Diseases: 4420
    - Spinal Muscular Atrophy: 2346
      - X-Linked Bulbo-Spinal Atrophy: 548
- Neuromuscular Diseases: 2048
  - Motor Neuron Disease: 1851
    - Spinal Muscular Atrophy: 2346
      - X-Linked Bulbo-Spinal Atrophy: 548
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Inborn Genetic Diseases: 12342
  - Nervous System Heredodegenerative Disorders: 62
    - X-Linked Bulbo-Spinal Atrophy: 548
  - X-Linked Genetic Diseases: 42
    - X-Linked Bulbo-Spinal Atrophy: 548

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Disease

Drug/Important Bio-Agent (IBA)