Concept information
Nervous System Diseases
Central Nervous System Diseases
Spinal Cord Diseases
Muscular Atrophy, Spinal
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Término preferido
Bulbo-Spinal Atrophy, X-Linked
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Tipo
-
mesh:Descriptor
Definición
- An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR.
Concepto genérico
Etiquetas alternativas
- Atrophy, Muscular, Spinobulbar
- 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
- Spinal And Bulbar Muscular Atrophy, X-Linked 1
- Spinobulbar Muscular Atrophy
- X-Linked Bulbo-Spinal Atrophy
- X-linked Bulbospinal Muscular Atrophy
- X-Linked Spinal and Bulbar Muscular Atrophy
En otras lenguas
-
francés
-
Amyotrophie bulbo-spinale héréditaire liée à l'X
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Amyotrophie bulbo-spinale liée à l'X
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Amyotrophie bulbospinale héréditaire liée à l'X
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Amyotrophie spino-bulbaire liée à l'X
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Amyotrophie spinobulbaire liée à l'X
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Atrophie bulbo-spinale liée à l'X
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Atrophie bulbospinale liée à l'X
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Atrophie musculaire spinale et bulbaire liée à l'X
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Maladie de Kennedy
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Syndrome de Kennedy
URI
http://data.loterre.fr/ark:/67375/JVR-HR1VJT6N-0
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