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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 .
C05.651.534.500.500 Myotonic Dystrophy .
C05.651.575 Myopathies, Structural, Congenital .
C05.651.662 Myotonic Disorders .
C05.651.662.750 Myotonic Dystrophy .
C10 Nervous System Diseases .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.547 Myotonic Dystrophy .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.175 Muscular Disorders, Atrophic .
C10.668.491.175.500 Muscular Dystrophies .
C10.668.491.175.500.500 Myotonic Dystrophy .
C10.668.491.550 Myopathies, Structural, Congenital .
C10.668.491.606 Myotonic Disorders .
C10.668.491.606.750 Myotonic Dystrophy .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.542 Myotonic Dystrophy .
C16.320.577 Muscular Dystrophies .
C16.320.577.500 Myotonic Dystrophy .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
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. .
1.00
2242
 
Myotonic Dystrophy .
Congenital Myotonic Dystrophy .
Dystrophia Myotonica 1 .
Dystrophia Myotonica 2 .
Myotonia Atrophica .
Myotonia Dystrophica .
Myotonic Dystrophy 1 .
Myotonic Dystrophy 2 .
PROMM (Proximal Myotonic Myopathy) .
Proximal Myotonic Myopathy .
Ricker Syndrome .
Steinert Myotonic Dystrophy .
Steinert's Disease .
Atrophica, Myotonia .
Atrophicas, Myotonia .
Congenital Myotonic Dystrophies .
Disease, Steinert .
Disease, Steinert's .
Dystrophia Myotonica 2s .
Dystrophia Myotonicas .
Dystrophica, Myotonia .
Dystrophicas, Myotonia .
Dystrophies, Congenital Myotonic .
Dystrophies, Myotonic .
Dystrophy, Congenital Myotonic .
Dystrophy, Myotonic .
Dystrophy, Steinert Myotonic .
Myopathies, Proximal Myotonic .
Myopathy, Proximal Myotonic .
Myotonia Atrophicas .
Myotonia Dystrophicas .
Myotonic Dystrophies .
Myotonic Dystrophies, Congenital .
Myotonic Dystrophy, Steinert .
Myotonic Myopathies, Proximal .
Myotonica, Dystrophia .
Myotonicas, Dystrophia .
PROMMs (Proximal Myotonic Myopathy) .
Proximal Myotonic Myopathies .
Steinerts Disease .
Syndrome, Ricker .
Dystrophia Myotonica .
Steinert Disease .
Myotonic Dystrophy, Congenital .
Myotonic Myopathy, Proximal .
MYOTONIA DYSTROPHICA .
STEINERT'S DISEASE .
MYOTONIA ATROPHICA .
Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2. .
0.86
1034355
 
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. .
0.84
34120488
 
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. .
0.80
7516