Categorias DeCS
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 .
C05.651.662 Myotonic Disorders .
C05.651.662.750 Myotonic Dystrophy .
C10 Nervous System Diseases .
C10.500 Nervous System Malformations .
C10.500.507 Malformations of Cortical Development .
C10.500.507.450 Malformations of Cortical Development, Group II .
C10.500.507.450.499 Lissencephaly .
C10.500.507.450.499.249 Cobblestone Lissencephaly .
C10.500.507.450.499.249.500 Walker-Warburg Syndrome .
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 .
C10.668.491.606 Myotonic Disorders .
C10.668.491.606.750 Myotonic Dystrophy .
C11 Eye Diseases .
C11.270 Eye Diseases, Hereditary .
C11.270.881 Walker-Warburg Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.666 Nervous System Malformations .
C16.131.666.507 Malformations of Cortical Development .
C16.131.666.507.450 Malformations of Cortical Development, Group II .
C16.131.666.507.450.499 Lissencephaly .
C16.131.666.507.450.499.249 Cobblestone Lissencephaly .
C16.131.666.507.450.499.249.500 Walker-Warburg Syndrome .
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 .
C16.320.577.750 Walker-Warburg Syndrome .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.210 Contractile Proteins .
D12.776.210.500 Muscle Proteins .
D12.776.210.500.410 Dystrophin-Associated Proteins .
D12.776.210.500.410.500 Dystroglycans .
D12.776.220 Cytoskeletal Proteins .
D12.776.220.362 Dystrophin-Associated Proteins .
D12.776.220.362.249 Dystroglycans .
D12.776.543 Membrane Proteins .
D12.776.543.268 Dystrophin-Associated Proteins .
D12.776.543.268.500 Dystroglycans .
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| | Termos
Sinônimos e Históricos | Documentos
LILACS e MDL | | | | | |
| Walker-Warburg Syndrome .
COD-MD Syndrome .
Cerebroocular Dysplasia-Muscular Dystrophy Syndrome .
Congenital Muscular Dystrophy-Dystroglycanopathy with Brain and Eye Anomalies, Type A1 .
Fukuyama CMD .
Fukuyama Muscular Dystrophy .
Fukuyama Syndrome .
HARD Syndrome .
Hydrocephalus, Agyria, And Retinal Dysplasia .
LGMD2K .
MDDGA1 .
MEB (Muscle-Eye-Brain) Syndrome .
Muscle Eye Brain Disease .
Muscle-Eye-Brain Disease, POMT1-Related .
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive, With Mental Retardation .
Muscular Dystrophy, Limb-Girdle, Type 2K .
Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies), Type A, 1 .
Muscular Dystrophy-Dystroglycanopathy (Limb-Girdle), Type C, 1 .
Pagon Syndrome .
CMD, Fukuyama .
COD MD Syndrome .
COD-MD Syndromes .
Cerebroocular Dysplasia Muscular Dystrophy Syndrome .
Congenital Muscular Dystrophy Dystroglycanopathy with Brain and Eye Anomalies, Type A1 .
Disease, POMT1-Related Muscle-Eye-Brain .
Diseases, POMT1-Related Muscle-Eye-Brain .
Dystrophy, Fukuyama Muscular .
HARD Syndromes .
Muscle Eye Brain Disease, POMT1 Related .
Muscle-Eye-Brain Diseases .
Muscle-Eye-Brain Diseases, POMT1-Related .
Muscular Dystrophy, Fukuyama .
POMT1-Related Muscle-Eye-Brain Disease .
POMT1-Related Muscle-Eye-Brain Diseases .
Pagon Syndromes .
Syndrome, COD-MD .
Syndrome, Chemke .
Syndrome, Fukuyama .
Syndrome, HARD .
Syndrome, Pagon .
Syndrome, Walker-Warburg .
Syndrome, Warburg .
Syndromes, COD-MD .
Syndromes, HARD .
Syndromes, Pagon .
Walker Warburg Syndrome .
alpha Dystroglycanopathies .
alpha-Dystroglycanopathies .
Cerebromuscular Dystrophy, Fukuyama Type .
Chemke Syndrome .
Fukuyama Congenital Muscular Dystrophy .
Fukuyama Type Congenital Muscular Dystrophy .
Muscle-Eye-Brain Disease .
Muscular Dystrophy, Congenital, Fukuyama Type .
Warburg Syndrome .
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| 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 .
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