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 DeCS Categories

C05 Musculoskeletal Diseases .
C05.651 Muscular Diseases .
C05.651.534 Muscular Disorders, Atrophic .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.854 Spinal Cord Diseases .
C10.228.854.468 Muscular Atrophy, Spinal .
C10.228.854.468.399 Bulbo-Spinal Atrophy, X-Linked .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.175 Bulbo-Spinal Atrophy, X-Linked .
C10.574.562 Motor Neuron Disease .
C10.574.562.500 Muscular Atrophy, Spinal .
C10.574.562.500.374 Bulbo-Spinal Atrophy, X-Linked .
C10.668 Neuromuscular Diseases .
C10.668.467 Motor Neuron Disease .
C10.668.467.500 Muscular Atrophy, Spinal .
C10.668.467.500.186 Bulbo-Spinal Atrophy, X-Linked .
C10.668.491 Muscular Diseases .
C10.668.491.175 Muscular Disorders, Atrophic .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.076 Bulbo-Spinal Atrophy, X-Linked .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Muscular Disorders, Atrophic .
Atrophic Muscular Disorders .
Spinal and Bulbar Muscular Atrophy .
Spinobulbar Atrophy .
Spinopontine Atrophy .
Atrophic Muscular Disorder .
Atrophies, Disuse .
Atrophies, Spinobulbar .
Atrophies, Spinobulbar Muscular .
Atrophies, Spinopontine .
Atrophy, Spinobulbar .
Atrophy, Spinobulbar Muscular .
Disorder, Atrophic Muscular .
Disorders, Atrophic Muscular .
Disuse Atrophies .
Disuse Atrophy .
Muscular Atrophies, Spinobulbar .
Muscular Disorder, Atrophic .
Spinobulbar Atrophies .
Spinobulbar Muscular Atrophies .
Spinopontine Atrophies .
Atrophy, Disuse .
Atrophy, Muscular, Spinobulbar .
Atrophy, Spinopontine .
Muscular Atrophy, Spinobulbar .
Spinobulbar Muscular Atrophy .
Disorders characterized by an abnormal reduction in muscle volume due to a decrease in the size or number of muscle fibers. Atrophy may result from diseases intrinsic to muscle tissue (e.g., MUSCULAR DYSTROPHY) or secondary to PERIPHERAL NERVOUS SYSTEM DISEASES that impair innervation to muscle tissue (e.g., MUSCULAR ATROPHY, SPINAL). .
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Bulbo-Spinal Atrophy, X-Linked .
Bulbospinal Muscular Atrophy, X-linked .
Kennedy Disease .
Kennedy Spinal and Bulbar Muscular Atrophy .
Kennedy's Disease .
Spinal And Bulbar Muscular Atrophy, X-Linked 1 .
X-Linked Bulbo-Spinal Atrophy .
X-Linked Spinal and Bulbar Muscular Atrophy .
X-linked Bulbospinal Muscular Atrophy .
Atrophies, X-Linked Bulbo-Spinal .
Atrophy, X-Linked Bulbo-Spinal .
Bulbo Spinal Atrophy, X Linked .
Bulbo-Spinal Atrophies, X-Linked .
Bulbospinal Muscular Atrophy, X linked .
Disease, Kennedy .
Disease, Kennedy's .
Kennedys Disease .
Spinal And Bulbar Muscular Atrophy, X Linked 1 .
Syndrome, Kennedy .
X Linked Bulbo Spinal Atrophy .
X Linked Spinal and Bulbar Muscular Atrophy .
X linked Bulbospinal Muscular Atrophy .
X-Linked Bulbo-Spinal Atrophies .
Kennedy Syndrome .
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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3123
 
Muscular Atrophy, Spinal .
Adult Spinal Muscular Atrophy .
Adult-Onset Spinal Muscular Atrophy .
Amyotrophy, Neurogenic Scapuloperoneal, New England Type .
Distal Spinal Muscular Atrophy .
Hereditary Motor Neuronopathy .
Muscular Atrophy, Adult Spinal .
Myelopathic Muscular Atrophy .
Myelopathic Muscular Atrophy, Progressive .
Progressive Myelopathic Muscular Atrophy .
Progressive Proximal Myelopathic Muscular Atrophy .
Proximal Myelopathic Muscular Atrophy, Progressive .
Scapuloperoneal Spinal Muscular Atrophy .
Spinal Amyotrophy .
Spinal Muscular Atrophy, Distal .
Spinal Muscular Atrophy, Oculopharyngeal .
Spinal Muscular Atrophy, Scapuloperoneal .
Spinal Muscular Atrophy, Scapuloperoneal Form .
Adult Onset Spinal Muscular Atrophy .
Amyotrophies, Spinal .
Amyotrophy, Spinal .
Atrophies, Progressive Muscular .
Atrophy, Myelopathic Muscular .
Atrophy, Progressive Muscular .
Atrophy, Spinal Muscular .
Bulbospinal Neuronopathies .
Hereditary Motor Neuronopathies .
Motor Neuronopathies, Hereditary .
Motor Neuronopathy, Hereditary .
Muscular Atrophies, Progressive .
Muscular Atrophy, Myelopathic .
Muscular Atrophy, Progressive .
Neuronopathies, Bulbospinal .
Neuronopathies, Hereditary Motor .
Neuronopathy, Bulbospinal .
Neuronopathy, Hereditary Motor .
Progressive Muscular Atrophies .
Spinal Amyotrophies .
Progressive Muscular Atrophy .
Spinal Muscular Atrophy .
Bulbospinal Neuronopathy .
Oculopharyngeal Spinal Muscular Atrophy .
Scapuloperoneal Form of Spinal Muscular Atrophy .
MYELOPATHIC MUSCULAR ATROPHY .
A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089) .
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