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 DeCS Categories

C05 Musculoskeletal Diseases .
C05.651 Muscular Diseases .
C05.651.534 Muscular Disorders, Atrophic .
C05.651.534.500 Muscular Dystrophies .
C05.651.534.500.074 Distal Myopathies .
C05.651.575 Myopathies, Structural, Congenital .
C05.651.575.290 Myopathies, Nemaline .
C05.651.662 Myotonic Disorders .
C10 Nervous System Diseases .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.175 Muscular Disorders, Atrophic .
C10.668.491.175.500 Muscular Dystrophies .
C10.668.491.175.500.074 Distal Myopathies .
C10.668.491.550 Myopathies, Structural, Congenital .
C10.668.491.550.290 Myopathies, Nemaline .
C10.668.491.606 Myotonic Disorders .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.577 Muscular Dystrophies .
C16.320.577.074 Distal Myopathies .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Muscular Diseases .
Myopathic Conditions .
Muscle Disorder .
Muscular Disease .
Myopathic Condition .
Myopathy .
Muscle Disorders .
Myopathies .
Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. .
1.00
32620488
 
Myotonic Disorders .
Eulenburg Disease .
Eulenburg's Disease .
Paralysis Periodica Paramyotonia .
Paramyotonia Congenita Without Cold Paralysis .
Paramyotonia Congenita of von Eulenberg .
Von Eulenberg's Disease .
Disorder, Myotonic .
Disorders, Myotonic .
Myopathy, Myotonic .
Myotonic Disorder .
Myotonic Myopathies .
Myotonic Myopathy .
Von Eulenberg Disease .
Myopathies, Myotonic .
Myotonia Fluctuans .
Paramyotonia Congenita .
Diseases characterized by MYOTONIA, which may be inherited or acquired. Myotonia may be restricted to certain muscles (e.g., intrinsic hand muscles) or occur as a generalized condition. .
0.83
2242
 
Myopathies, Structural, Congenital .
Autosomal Dominant Myotubular Myopathy .
Autosomal Recessive Centronuclear Myopathy .
CFTDM .
Congenital Fiber-Type Disproportion .
Congenital Myopathy with Fiber Type Disproportion .
Congenital Non-Progressive Myopathies .
Congenital Structural Myopathies .
Fiber-Type Disproportion Myopathy, Congenital .
Myopathy, Centronuclear, 1 .
Myopathy, Centronuclear, Autosomal Dominant .
Myopathy, Congenital, With Fiber-Type Disproportion .
Myopathy, Tubular Aggregate .
Myotubular Myopathy .
Myotubular Myopathy 1 .
Myotubular Myopathy, Autosomal Dominant .
Myotubular Myopathy, X-Linked .
Non-Progressive Myopathies, Congenital .
Structural Myopathies, Congenital .
X-Linked Centronuclear Myopathy .
X-Linked Myotubular Myopathy .
XLMTM .
Aggregate Myopathies, Tubular .
Aggregate Myopathy, Tubular .
Centronuclear Myopathies .
Centronuclear Myopathies, X-Linked .
Centronuclear Myopathy, X-Linked .
Congenital Fiber-Type Disproportions .
Congenital Non Progressive Myopathies .
Congenital Non-Progressive Myopathy .
Congenital Structural Myopathy .
Disproportion, Congenital Fiber-Type .
Disproportions, Congenital Fiber-Type .
Fiber Type Disproportion Myopathy, Congenital .
Fiber-Type Disproportion, Congenital .
Fiber-Type Disproportions, Congenital .
Myopathies, Centronuclear .
Myopathies, Congenital Non-Progressive .
Myopathies, Congenital Structural .
Myopathies, Myotubular .
Myopathies, Tubular Aggregate .
Myopathies, X-Linked Centronuclear .
Myopathies, X-Linked Myotubular .
Myopathy, Centronuclear .
Myopathy, Congenital Non-Progressive .
Myopathy, Congenital Structural .
Myopathy, X-Linked Centronuclear .
Myopathy, X-Linked Myotubular .
Myotubular Myopathies .
Myotubular Myopathies, X-Linked .
Myotubular Myopathy, X Linked .
Non Progressive Myopathies, Congenital .
Non-Progressive Myopathy, Congenital .
Structural Myopathy, Congenital .
Tubular Aggregate Myopathies .
X Linked Centronuclear Myopathy .
X Linked Myotubular Myopathy .
X-Linked Centronuclear Myopathies .
X-Linked Myotubular Myopathies .
Centronuclear Myopathy .
Congenital Fiber Type Disproportion .
Myopathy, Myotubular .
Tubular Aggregate Myopathy .
A heterogeneous group of diseases characterized by the early onset of hypotonia, developmental delay of motor skills, non-progressive weakness. Each of these disorders is associated with a specific histologic muscle fiber abnormality. .
0.78
7516
 
Distal Myopathies .
Distal Muscular Dystrophies .
Distal Myopathy .
Distal Myopathy 1 .
Distal Myopathy Markesbery-Griggs Type .
Finnish-Markesbery Muscular Dystrophy .
Laing Distal Myopathy .
Laing Early-Onset Distal Myopathy .
Muscular Dystrophy, Distal, Late-Onset, Autosomal Dominant .
Myopathy, Distal 1 .
Myopathy, Distal, Early-Onset, Autosomal Dominant .
Myopathy, Distal, Swedish .
Myopathy, Late Distal Hereditary .
Tardive Tibial Muscular Dystrophy .
Tibial Muscular Dystrophy .
Tibial Muscular Dystrophy, Tardive .
Udd Distal Myopathy .
Udd Myopathy .
Udd-Markesbery Muscular Dystrophy .
Welander Distal Myopathy .
Distal 1 Myopathies .
Distal 1 Myopathy .
Distal Muscular Dystrophy .
Distal Myopathy 1s .
Distal Myopathy Markesbery Griggs Type .
Distal Myopathy, Laing .
Distal Myopathy, Udd .
Distal Myopathy, Welander .
Finnish Markesbery Muscular Dystrophy .
Laing Early Onset Distal Myopathy .
Muscular Dystrophies, Distal .
Muscular Dystrophies, Tibial .
Muscular Dystrophy, Finnish-Markesbery .
Muscular Dystrophy, Tibial .
Muscular Dystrophy, Udd-Markesbery .
Myopathies, Distal .
Myopathies, Distal 1 .
Myopathy 1, Distal .
Myopathy 1s, Distal .
Myopathy, Distal .
Myopathy, Laing Distal .
Myopathy, Udd .
Myopathy, Udd Distal .
Udd Markesbery Muscular Dystrophy .
Muscular Dystrophy, Distal .
A heterogeneous group of genetic disorders characterized by progressive MUSCULAR ATROPHY and MUSCLE WEAKNESS beginning in the hands, the legs, or the feet. Most are adult-onset autosomal dominant forms. Others are autosomal recessive. .
0.78
4223
 
Myopathies, Nemaline .
Adult Onset Nemaline Myopathy .
Autosomal Dominant Nemaline Myopathy .
Autosomal Recessive Nemaline Myopathy .
Childhood Onset Nemaline Myopathy .
Late Onset Nemaline Myopathy .
Nemaline Body Disease .
Nemaline Myopathy .
Nemaline Myopathy, Adult Onset .
Nemaline Myopathy, Autosomal Dominant .
Nemaline Myopathy, Autosomal Recessive .
Nemaline Myopathy, Childhood Onset .
Nemaline Myopathy, Late Onset .
Nemaline Rod Disease .
Rod Body Disease .
Rod Myopathy .
Rod-Body Myopathy .
Myopathies, Rod .
Myopathies, Rod-Body .
Myopathy, Rod Body .
Rod Body Myopathy .
Rod Myopathies .
Rod-Body Myopathies .
Myopathy, Nemaline .
Myopathy, Rod .
Nemaline Myopathies .
Myopathy, Rod-Body .
CENTRAL CORE DISEASE .
ROD MYOPATHY .
NEMALINE MYOPATHY .
A group of inherited congenital myopathic conditions characterized clinically by weakness, hypotonia, and prominent hypoplasia of proximal muscles including the face. Muscle biopsy reveals large numbers of rod-shaped structures beneath the muscle fiber plasma membrane. This disorder is genetically heterogeneous and may occasionally present in adults. (Adams et al., Principles of Neurology, 6th ed, p1453) .
0.77
8432