Bulbo-Spinal Atrophy, X-Linked
An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR.
Year introduced: 2009(2000)
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Subheadings:
Tree Number(s): C10.228.854.468.399, C10.574.500.175, C10.574.562.500.374, C10.668.467.500.186, C16.320.322.076, C16.320.400.100
MeSH Unique ID: D055534
Entry Terms:
- Bulbo Spinal Atrophy, X Linked
- Kennedy Syndrome
- X-Linked Bulbo-Spinal Atrophy
- Atrophies, X-Linked Bulbo-Spinal
- Atrophy, X-Linked Bulbo-Spinal
- Bulbo-Spinal Atrophies, X-Linked
- X-Linked Bulbo-Spinal Atrophies
- X Linked Bulbo Spinal Atrophy
- Atrophy, Muscular, Spinobulbar
- Muscular Atrophy, Spinobulbar
- Atrophy, Spinobulbar Muscular
- Spinobulbar Muscular Atrophies
- Spinobulbar Muscular Atrophy
- Kennedy Disease
- Bulbospinal Muscular Atrophy, X-linked
- Bulbospinal Muscular Atrophy, X linked
- Kennedy Spinal and Bulbar Muscular Atrophy
- Spinal and Bulbar Muscular Atrophy
- X-linked Bulbospinal Muscular Atrophy
- X linked Bulbospinal Muscular Atrophy
- Kennedy's Disease
- Spinal And Bulbar Muscular Atrophy, X-Linked 1
- Spinal And Bulbar Muscular Atrophy, X Linked 1
- X-Linked Spinal and Bulbar Muscular Atrophy
- X Linked Spinal and Bulbar Muscular Atrophy