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2007 MeSH

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Muscular Dystrophies
MeSH HeadingMuscular Dystrophies
Tree NumberC05.651.534.500
Tree NumberC10.668.491.175.500
Tree NumberC16.320.577
AnnotationGEN: prefer specifics; do not confuse with MYOTONIC DYSTROPHY
Scope NoteA heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS.
Entry TermMuscular Dystrophy
Entry TermMyodystrophica
Entry TermMyodystrophy
See AlsoMice, Inbred mdx
Allowable QualifiersBL CF CI CL CN CO DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RA RH RI RT SU TH UR US VI
History Note2000(1966)
Entry Combinationveterinary:Muscular Dystrophy, Animal
Date of Entry19991108
Unique IDD009136


MeSH Tree Structures

 
Musculoskeletal Diseases [C05]
   Muscular Diseases [C05.651]
      Muscular Disorders, Atrophic [C05.651.534]
Muscular Dystrophies [C05.651.534.500]
Distal Myopathies [C05.651.534.500.074]
Glycogen Storage Disease Type VII [C05.651.534.500.149]
Muscular Dystrophies, Limb-Girdle [C05.651.534.500.280]
Muscular Dystrophy, Duchenne [C05.651.534.500.300]
Muscular Dystrophy, Emery-Dreifuss [C05.651.534.500.350]
Muscular Dystrophy, Facioscapulohumeral [C05.651.534.500.400]
Muscular Dystrophy, Oculopharyngeal [C05.651.534.500.450]
Myotonic Dystrophy [C05.651.534.500.500]
Postpoliomyelitis Syndrome [C05.651.534.750]

 
Nervous System Diseases [C10]
   Neuromuscular Diseases [C10.668]
      Muscular Diseases [C10.668.491]
         Muscular Disorders, Atrophic [C10.668.491.175]
Muscular Dystrophies [C10.668.491.175.500]
Distal Myopathies [C10.668.491.175.500.074]
Muscular Dystrophies, Limb-Girdle [C10.668.491.175.500.149]
Muscular Dystrophy, Duchenne [C10.668.491.175.500.300]
Muscular Dystrophy, Emery-Dreifuss [C10.668.491.175.500.350]
Muscular Dystrophy, Facioscapulohumeral [C10.668.491.175.500.400]
Muscular Dystrophy, Oculopharyngeal [C10.668.491.175.500.450]
Myotonic Dystrophy [C10.668.491.175.500.500]
Postpoliomyelitis Syndrome [C10.668.491.175.750]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Genetic Diseases, Inborn [C16.320]
Adrenal Hyperplasia, Congenital [C16.320.033]
Anemia, Hemolytic, Congenital [C16.320.070]  +
Anemia, Hypoplastic, Congenital [C16.320.077]  +
Ataxia Telangiectasia [C16.320.080]
Blood Coagulation Disorders, Inherited [C16.320.099]  +
Brugada Syndrome [C16.320.100]
CADASIL [C16.320.129]
Camurati-Engelmann Syndrome [C16.320.144]
Cardiomyopathy, Hypertrophic, Familial [C16.320.160]
Cherubism [C16.320.170]
Chromosome Disorders [C16.320.180]  +
Cystic Fibrosis [C16.320.190]
Dwarfism [C16.320.240]  +
Eye Diseases, Hereditary [C16.320.290]  +
Familial Mediterranean Fever [C16.320.306]
Genetic Diseases, X-Linked [C16.320.322]  +
Genetic Diseases, Y-Linked [C16.320.338]
Hajdu-Cheney Syndrome [C16.320.355]
Hemoglobinopathies [C16.320.365]  +
Heredodegenerative Disorders, Nervous System [C16.320.400]  +
Hyperthyroxinemia, Familial Dysalbuminemic [C16.320.427]
Jervell-Lange Nielsen Syndrome [C16.320.455]
Kallmann Syndrome [C16.320.467]
Kartagener Syndrome [C16.320.480]
Marfan Syndrome [C16.320.540]
Metabolism, Inborn Errors [C16.320.565]  +
Muscular Dystrophies [C16.320.577]
Distal Myopathies [C16.320.577.074]
Glycogen Storage Disease Type VII [C16.320.577.149]
Muscular Dystrophies, Limb-Girdle [C16.320.577.280]
Muscular Dystrophy, Duchenne [C16.320.577.300]
Muscular Dystrophy, Emery-Dreifuss [C16.320.577.350]
Muscular Dystrophy, Facioscapulohumeral [C16.320.577.400]
Muscular Dystrophy, Oculopharyngeal [C16.320.577.450]
Myotonic Dystrophy [C16.320.577.500]
Myasthenic Syndromes, Congenital [C16.320.590]
Nail-Patella Syndrome [C16.320.600]
Neoplastic Syndromes, Hereditary [C16.320.700]  +
Osteogenesis Imperfecta [C16.320.737]
Pain Insensitivity, Congenital [C16.320.775]
Romano-Ward Syndrome [C16.320.800]
Skin Diseases, Genetic [C16.320.850]  +
Werner Syndrome [C16.320.925]

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