| Descriptor English: | Bulbo-Spinal Atrophy, X-Linked | ||||||
| Descriptor Spanish: |
Atrofia Bulboespinal Ligada al X
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| Descriptor Portuguese: | Atrofia Bulboespinal Ligada ao X | ||||||
| Descriptor French: | Amyotrophie bulbospinale liée à l'X | ||||||
| Entry term(s): |
Atrophies, X-Linked Bulbo-Spinal Atrophy, Muscular, Spinobulbar Atrophy, Spinobulbar Muscular Atrophy, X-Linked Bulbo-Spinal Bulbo Spinal Atrophy, X Linked Bulbo-Spinal Atrophies, X-Linked Bulbospinal Muscular Atrophy, X linked Bulbospinal Muscular Atrophy, X-linked Kennedy Disease Kennedy Spinal and Bulbar Muscular Atrophy Kennedy Syndrome Kennedy's Disease Muscular Atrophy, Spinobulbar Spinal And Bulbar Muscular Atrophy, X Linked 1 Spinal And Bulbar Muscular Atrophy, X-Linked 1 Spinal and Bulbar Muscular Atrophy Spinobulbar Muscular Atrophies Spinobulbar Muscular Atrophy X Linked Bulbo Spinal Atrophy X Linked Spinal and Bulbar Muscular Atrophy X linked Bulbospinal Muscular Atrophy X-Linked Bulbo-Spinal Atrophies X-Linked Bulbo-Spinal Atrophy X-Linked Spinal and Bulbar Muscular Atrophy X-linked Bulbospinal Muscular Atrophy |
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| 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 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D055534 | ||||||
| Scope note: | An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 2009; see MUSCULAR ATROPHY, SPINAL 2000-2008 |
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| History Note: | 2009(2000); use MUSCULAR ATROPHY, SPINAL 2000-2008 |
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| DeCS ID: | 53093 | ||||||
| Unique ID: | D055534 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2009/01/01 | ||||||
| Date of Entry: | 2008/07/08 | ||||||
| Revision Date: | 2018/06/29 |
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Bulbo-Spinal Atrophy, X-Linked
- Preferred
| Concept UI |
M0518289 |
| Scope note | An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR. |
| Preferred term | Bulbo-Spinal Atrophy, X-Linked |
| Entry term(s) |
Atrophies, X-Linked Bulbo-Spinal Atrophy, Muscular, Spinobulbar Atrophy, Spinobulbar Muscular Atrophy, X-Linked Bulbo-Spinal Bulbo Spinal Atrophy, X Linked Bulbo-Spinal Atrophies, X-Linked Bulbospinal Muscular Atrophy, X linked Bulbospinal Muscular Atrophy, X-linked Kennedy Disease Kennedy Spinal and Bulbar Muscular Atrophy Kennedy Syndrome Kennedy's Disease Muscular Atrophy, Spinobulbar Spinal And Bulbar Muscular Atrophy, X Linked 1 Spinal And Bulbar Muscular Atrophy, X-Linked 1 Spinal and Bulbar Muscular Atrophy Spinobulbar Muscular Atrophies Spinobulbar Muscular Atrophy X Linked Bulbo Spinal Atrophy X Linked Spinal and Bulbar Muscular Atrophy X linked Bulbospinal Muscular Atrophy X-Linked Bulbo-Spinal Atrophies X-Linked Bulbo-Spinal Atrophy X-Linked Spinal and Bulbar Muscular Atrophy X-linked Bulbospinal Muscular Atrophy |
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