Bulbo-Spinal Atrophy, X-Linked
"Bulbo-Spinal Atrophy, X-Linked" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR.
| Descriptor ID |
D055534
|
| MeSH 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
|
| Concept/Terms |
Bulbo-Spinal Atrophy, X-Linked- Bulbo-Spinal Atrophy, X-Linked
- Atrophies, X-Linked Bulbo-Spinal
- Atrophy, X-Linked Bulbo-Spinal
- Bulbo Spinal Atrophy, X Linked
- Bulbo-Spinal Atrophies, X-Linked
- X-Linked Bulbo-Spinal Atrophies
- Kennedy Disease
- Disease, Kennedy
- Kennedy Spinal and Bulbar Muscular Atrophy
- Kennedy Syndrome
- Syndrome, Kennedy
- X-Linked Bulbo-Spinal Atrophy
- X Linked Bulbo Spinal Atrophy
- X-linked Bulbospinal Muscular Atrophy
- X linked Bulbospinal Muscular Atrophy
- Kennedy's Disease
- Disease, Kennedy's
- Kennedys Disease
- X-Linked Spinal and Bulbar Muscular Atrophy
- X Linked Spinal and Bulbar Muscular Atrophy
- Bulbospinal Muscular Atrophy, X-linked
- Bulbospinal Muscular Atrophy, X linked
- Spinal And Bulbar Muscular Atrophy, X-Linked 1
- Spinal And Bulbar Muscular Atrophy, X Linked 1
|
Below are MeSH descriptors whose meaning is more general than "Bulbo-Spinal Atrophy, X-Linked".
- Diseases [C]
- Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
- Spinal Cord Diseases [C10.228.854]
- Muscular Atrophy, Spinal [C10.228.854.468]
- Bulbo-Spinal Atrophy, X-Linked [C10.228.854.468.399]
- Neurodegenerative Diseases [C10.574]
- Heredodegenerative Disorders, Nervous System [C10.574.500]
- Bulbo-Spinal Atrophy, X-Linked [C10.574.500.175]
- Motor Neuron Disease [C10.574.562]
- Muscular Atrophy, Spinal [C10.574.562.500]
- Bulbo-Spinal Atrophy, X-Linked [C10.574.562.500.374]
- Neuromuscular Diseases [C10.668]
- Motor Neuron Disease [C10.668.467]
- Muscular Atrophy, Spinal [C10.668.467.500]
- Bulbo-Spinal Atrophy, X-Linked [C10.668.467.500.186]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Genetic Diseases, X-Linked [C16.320.322]
- Bulbo-Spinal Atrophy, X-Linked [C16.320.322.076]
Below are MeSH descriptors whose meaning is more specific than "Bulbo-Spinal Atrophy, X-Linked".
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