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 Categorias DeCS

C05 Musculoskeletal Diseases .
C05.550 Joint Diseases .
C05.550.150 Arthrogryposis .
C05.651 Muscular Diseases .
C05.651.102 Arthrogryposis .
C05.651.534 Muscular Disorders, Atrophic .
C05.651.534.500 Muscular Dystrophies .
C05.651.534.500.500 Myotonic Dystrophy .
C05.651.662 Myotonic Disorders .
C05.651.662.500 Myotonia Congenita .
C05.651.662.750 Myotonic Dystrophy .
C05.660 Musculoskeletal Abnormalities .
C05.660.077 Arthrogryposis .
C10 Nervous System Diseases .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.545 Myotonia Congenita .
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 .
C10.668.491.606 Myotonic Disorders .
C10.668.491.606.500 Myotonia Congenita .
C10.668.491.606.750 Myotonic Dystrophy .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.621 Musculoskeletal Abnormalities .
C16.131.621.077 Arthrogryposis .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.540 Myotonia Congenita .
C16.320.400.542 Myotonic Dystrophy .
C16.320.577 Muscular Dystrophies .
C16.320.577.500 Myotonic Dystrophy .
 
 Termos
 Sinônimos e Históricos		Documentos
LILACS e MDL		 
Neuromuscular Diseases .
Cramp-Fasciculation Syndrome .
Fasciculation-Cramp Syndrome, Benign .
Foley-Denny-Brown Syndrome .
Oppenheim's Disease .
Benign Fasciculation-Cramp Syndrome .
Benign Fasciculation-Cramp Syndromes .
Cramp Fasciculation Syndrome .
Cramp-Fasciculation Syndromes .
Fasciculation Cramp Syndrome, Benign .
Fasciculation-Cramp Syndromes, Benign .
Foley Denny Brown Syndrome .
Neuromuscular Disease .
Oppenheims Disease .
Syndrome, Cramp-Fasciculation .
Syndrome, Foley-Denny-Brown .
Syndromes, Cramp-Fasciculation .
Amyotonia Congenita .
Oppenheim Disease .
MYATONIA CONGENITA .
OPPENHEIM'S DISEASE .
1.00
2389320
 
Myotonia Congenita .
Batten Turner Congenital Myopathy .
Batten-Turner Congenital Myopathy .
Becker Disease .
Congenital Myotonia .
Generalized Myotonia of Becker .
Generalized Myotonia of Thomsen .
Myopathy, Congenital .
Myotonia Congenita, Autosomal Dominant .
Myotonia Congenita, Autosomal Recessive .
Myotonia Levior .
Myotonia, Generalized .
Thomsen's Disease .
Thomsens Disease .
Disease, Becker .
Disease, Thomsen .
Disease, Thomsen's .
Disease, Thomsens .
Generalized Myotonia .
Generalized Myotonia, Becker .
Generalized Myotonias .
Myotonia, Becker Generalized .
Myotonias, Generalized .
Thomsen Generalized Myotonia .
Thomsen Disease .
Becker Generalized Myotonia .
Myotonia, Generalized, Becker .
THOMSEN'S DISEASE .
0.74
14753
 
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 .
0.74
2242
 
Arthrogryposis .
Arthrogryposis Multiplex Congenita .
Arthrogryposis Multiplex Congenita (AMC) .
Congenital Arthromyodysplasia .
Congenital Multiple Arthrogryposis .
Fibrous Ankylosis of Multiple Joints .
Guérin-Stern Syndrome .
Otto Syndrome .
Rocher-Sheldon Syndrome .
Rossi Syndrome .
Arthrogryposes .
Arthrogryposes, Congenital Multiple .
Arthrogryposis Multiplex Congenitas .
Arthrogryposis Multiplex Congenitas (AMC) .
Arthrogryposis, Congenital Multiple .
Arthromyodysplasias, Congenital .
Congenita, Arthrogryposis Multiplex .
Congenita, Arthrogryposis Multiplex (AMC) .
Congenital Arthromyodysplasias .
Congenital Multiple Arthrogryposes .
Congenitas, Arthrogryposis Multiplex .
Congenitas, Arthrogryposis Multiplex (AMC) .
Guerin Stern Syndrome .
Guérin Stern Syndrome .
Multiple Arthrogryposes, Congenital .
Multiple Arthrogryposis, Congenital .
Multiplex Congenita, Arthrogryposis .
Multiplex Congenita, Arthrogryposis (AMC) .
Multiplex Congenitas, Arthrogryposis .
Multiplex Congenitas, Arthrogryposis (AMC) .
Rocher Sheldon Syndrome .
Syndrome, Guerin-Stern .
Syndrome, Guérin-Stern .
Syndrome, Otto .
Syndrome, Rocher-Sheldon .
Syndrome, Rossi .
Amyoplasia Congenita .
Arthromyodysplasia, Congenital .
Myodystrophia Fetalis Deformans .
Guerin-Stern Syndrome .
0.74
731592
 
/congenital .
/connatal .
/innate .
0.62
 
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 .
0.55
1014355