ONKI3 | Medical Subject Headings

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Muscular Dystrophies

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Muscular Dystrophies 35 coordinate concepts 9 subordinate concepts ∟ D009136Q000662* \| ∟ Distal Myopathies \| ∟ Glycogen Storage Disease Type VII \| ∟ Muscular Dystrophies, Limb-Girdle \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Muscular Dystrophy, Facioscapulohumeral \| ∟ Muscular Dystrophy, Oculopharyngeal \| ∟ Myotonic Dystrophy ∟ Postpoliomyelitis Syndrome \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Muscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies 35 coordinate concepts 9 subordinate concepts ∟ D009136Q000662* \| ∟ Distal Myopathies \| ∟ Glycogen Storage Disease Type VII \| ∟ Muscular Dystrophies, Limb-Girdle \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Muscular Dystrophy, Facioscapulohumeral \| ∟ Muscular Dystrophy, Oculopharyngeal \| ∟ Myotonic Dystrophy ∟ Postpoliomyelitis Syndrome \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies 35 coordinate concepts 9 subordinate concepts ∟ D009136Q000662* \| ∟ Distal Myopathies \| ∟ Glycogen Storage Disease Type VII \| ∟ Muscular Dystrophies, Limb-Girdle \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Muscular Dystrophy, Facioscapulohumeral \| ∟ Muscular Dystrophy, Oculopharyngeal \| ∟ Myotonic Dystrophy ∟ Postpoliomyelitis Syndrome \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies 35 coordinate concepts 9 subordinate concepts ∟ D009136Q000662* \| ∟ Distal Myopathies \| ∟ Glycogen Storage Disease Type VII \| ∟ Muscular Dystrophies, Limb-Girdle \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Muscular Dystrophy, Facioscapulohumeral \| ∟ Muscular Dystrophy, Oculopharyngeal \| ∟ Myotonic Dystrophy ∟ Postpoliomyelitis Syndrome \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Muscular Dystrophies Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Muscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neuromuscular Diseases ∟ Muscular Disorders, Atrophic ∟ Muscular Dystrophies Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Muscular Disorders, Atrophic > Muscular Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Muscular Disorders, Atrophic > Muscular Diseases > Neuromuscular Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) Muscular Disorders, Atrophic > Neuromuscular Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	D009136Q000662* \| Distal Myopathies \| Glycogen Storage Disease Type VII \| Muscular Dystrophies, Limb-Girdle \| Muscular Dystrophy, Duchenne \| Muscular Dystrophy, Emery-Dreifuss \| Muscular Dystrophy, Facioscapulohumeral \| Muscular Dystrophy, Oculopharyngeal \| Myotonic Dystrophy X
Annotation:	GEN: prefer specifics; do not confuse with MYOTONIC DYSTROPHY X
historyNote*:	2000(1966) X
publicMeSHNote*:	2000; see MUSCULAR DYSTROPHY 1966-1999 X
Scope note:	A 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. X
activeMeSHYear*:	2005 \| 2006 \| 2007X
dateCreated*:	1999-11-08X
dateRevised*:	2004-07-07X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Related term:	Mice, Inbred mdx X
Type:	Concept X
Coordinate terms:	Postpoliomyelitis Syndrome \| Adrenal Hyperplasia, Congenital \| Anemia, Hemolytic, Congenital \| Anemia, Hypoplastic, Congenital \| Ataxia Telangiectasia \| Blood Coagulation Disorders, Inherited \| Brugada Syndrome \| CADASIL \| Camurati-Engelmann Syndrome \| Cardiomyopathy, Hypertrophic, Familial \| Cherubism \| Chromosome Disorders \| Cystic Fibrosis \| Dwarfism \| Eye Diseases, Hereditary \| Familial Mediterranean Fever \| Genetic Diseases, X-Linked \| Genetic Diseases, Y-Linked \| Hajdu-Cheney Syndrome \| Hemoglobinopathies \| Heredodegenerative Disorders, Nervous System \| Hyperthyroxinemia, Familial Dysalbuminemic \| Jervell-Lange Nielsen Syndrome \| Kallmann Syndrome \| Kartagener Syndrome \| Marfan Syndrome \| Metabolism, Inborn Errors \| Myasthenic Syndromes, Congenital \| Nail-Patella Syndrome \| Neoplastic Syndromes, Hereditary \| Osteogenesis Imperfecta \| Pain Insensitivity, Congenital \| Romano-Ward Syndrome \| Skin Diseases, Genetic \| Werner Syndrome X
URI:	X
Labels and equivalent concepts:	Lihasdystrofiat (fi) Lihassurkastumataudit (fi, replaced) Lihassurkastumat (fi, replaced) Lihassurkastumatauti (fi, replaced) Lihassurkastuma (fi, replaced) Lihasrappeumat (fi, replaced) Lihasdystrofia (fi, replaced) Lihasrappeuma (fi, replaced) Muskeldystrofier (sv) Myodystrophica (en, replaced) Myodystrophy (en, replaced) Muscular Dystrophy (en, replaced) Dystrophia muscularis (la-FI, replaced) Dystrophia musculorum (la-FI, replaced) X
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