Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Preferred term
Bulbo-Spinal Atrophy, X-Linked
Type
-
Topical Descriptor
Broader concept
Entry terms
- Atrophies, X-Linked Bulbo-Spinal
- Atrophy, Muscular, Spinobulbar
- Atrophy, Spinobulbar Muscular
- Atrophy, X-Linked Bulbo-Spinal
- Bulbo-Spinal Atrophies, X-Linked
- Bulbospinal Muscular Atrophy, X linked
- Bulbospinal Muscular Atrophy, X-linked
- Kennedy Disease
- Kennedy's Disease
- Kennedy Spinal and Bulbar Muscular Atrophy
- Kennedy Syndrome
- Muscular Atrophy, Spinobulbar
- Spinal and Bulbar Muscular Atrophy
- Spinal And Bulbar Muscular Atrophy, X Linked 1
- Spinal And Bulbar Muscular Atrophy, X-Linked 1
- Spinobulbar Muscular Atrophies
- Spinobulbar Muscular Atrophy
- X-Linked Bulbo-Spinal Atrophies
- X Linked Bulbo Spinal Atrophy
- X-Linked Bulbo-Spinal Atrophy
- X linked Bulbospinal Muscular Atrophy
- X-linked Bulbospinal Muscular Atrophy
- X Linked Spinal and Bulbar Muscular Atrophy
- X-Linked Spinal and Bulbar Muscular Atrophy
Scope note
- An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR.
History note
- 2009(2000); use MUSCULAR ATROPHY, SPINAL 2000-2008
In other languages
URI
http://www.yso.fi/onto/mesh/D055534
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