Muscular Dystrophies [svalové dystrofie]

topical
141
Terms

muskulární dystrofie
myodystrofie

 

Muscular Dystrophy
Myodystrophica
Myodystrophy

Persistent link   https://www.medvik.cz/link/D009136
Definition

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.

Annotation
general or unspecified; prefer specifics; do not confuse with MYOTONIC DYSTROPHY
DUI
D009136 MeSH Browser
CUI
M0014254
History note
2000(1966)
Public note
2000; see MUSCULAR DYSTROPHY 1966-1999

Combination

veterinary
Muscular Dystrophy, Animal

Allowable subheadings

BL
blood 4
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 14
CO
complications 15
CN
congenital 7
DI
diagnosis 45
DG
diagnostic imaging 3
DH
diet therapy
DT
drug therapy 4
EC
economics
EM
embryology
EN
enzymology 1
EP
epidemiology 4
EH
ethnology
ET
etiology 15
GE
genetics 43
HI
history
IM
immunology
ME
metabolism 1
MI
microbiology
MO
mortality
NU
nursing 2
PS
parasitology
PA
pathology 11
PP
physiopathology 9
PC
prevention & control 1
PX
psychology
RT
radiotherapy
RH
rehabilitation 7
SU
surgery 1
TH
therapy 23
UR
urine
VI
virology

C Diseases
C05 Musculoskeletal Diseases 1 125
C05.651 Muscular Diseases 557
C05.651.534 Muscular Disorders, Atrophic 45
C05.651.534.500 Muscular Dystrophies 141
C05.651.534.500.074 Distal Myopathies 3
C05.651.534.500.149 Glycogen Storage Disease Type VII
C05.651.534.500.280 Muscular Dystrophies, Limb-Girdle 22
C05.651.534.500.300 Muscular Dystrophy, Duchenne 136
C05.651.534.500.350 Muscular Dystrophy, Emery-Dreifuss 18
C05.651.534.500.400 Muscular Dystrophy, Facioscapulohumeral 19
C05.651.534.500.450 Muscular Dystrophy, Oculopharyngeal 3
C05.651.534.500.500 Myotonic Dystrophy 96
C05.651.534.750 Postpoliomyelitis Syndrome 26
C10 Nervous System Diseases 1 884
C10.668 Neuromuscular Diseases 333
C10.668.491 Muscular Diseases 557
C10.668.491.175 Muscular Disorders, Atrophic 45
C10.668.491.175.500 Muscular Dystrophies 141
C10.668.491.175.500.074 Distal Myopathies 3
C10.668.491.175.500.112 Glycogen Storage Disease Type VII
C10.668.491.175.500.149 Muscular Dystrophies, Limb-Girdle 22
C10.668.491.175.500.300 Muscular Dystrophy, Duchenne 136
C10.668.491.175.500.350 Muscular Dystrophy, Emery-Dreifuss 18
C10.668.491.175.500.400 Muscular Dystrophy, Facioscapulohumeral 19
C10.668.491.175.500.450 Muscular Dystrophy, Oculopharyngeal 3
C10.668.491.175.500.500 Myotonic Dystrophy 96
C10.668.491.175.750 Postpoliomyelitis Syndrome 26
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 215
C16.320.033 Adrenal Hyperplasia, Congenital 226
C16.320.051 Alagille Syndrome 19
C16.320.060 alpha 1-Antitrypsin Deficiency 86
C16.320.070 Anemia, Hemolytic, Congenital 48
C16.320.077 Anemia, Hypoplastic, Congenital 3
C16.320.080 Ataxia Telangiectasia 48
C16.320.089 Autoimmune Lymphoproliferative Syndrome 2
C16.320.099 Blood Coagulation Disorders, Inherited 64
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.144 Camurati-Engelmann Syndrome 6
C16.320.160 Cardiomyopathy, Hypertrophic, Familial 33
C16.320.165 CHARGE Syndrome 1
C16.320.170 Cherubism 1
C16.320.180 Chromosome Disorders 260
C16.320.184 Ciliopathies 9
C16.320.188 Costello Syndrome 3
C16.320.190 Cystic Fibrosis 1 330
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 99
C16.320.290 Eye Diseases, Hereditary 58
C16.320.298 Familial Multiple Lipomatosis
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 2
C16.320.322 Genetic Diseases, X-Linked 60
C16.320.338 Genetic Diseases, Y-Linked 1
C16.320.355 Hajdu-Cheney Syndrome 6
C16.320.365 Hemoglobinopathies 68
C16.320.382 Hereditary Autoinflammatory Diseases 47
C16.320.400 Heredodegenerative Disorders, Nervous System 46
C16.320.413 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.427 Hyperthyroxinemia, Familial Dysalbuminemic 2
C16.320.447 Imprinting Disorders
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.495 Lennox Gastaut Syndrome 6
C16.320.510 Loeys-Dietz Syndrome 7
C16.320.540 Marfan Syndrome 105
C16.320.565 Metabolism, Inborn Errors 714
C16.320.577 Muscular Dystrophies 141
C16.320.577.074 Distal Myopathies 3
C16.320.577.149 Glycogen Storage Disease Type VII
C16.320.577.280 Muscular Dystrophies, Limb-Girdle 22
C16.320.577.300 Muscular Dystrophy, Duchenne 136
C16.320.577.350 Muscular Dystrophy, Emery-Dreifuss 18
C16.320.577.400 Muscular Dystrophy, Facioscapulohumeral 19
C16.320.577.450 Muscular Dystrophy, Oculopharyngeal 3
C16.320.577.500 Myotonic Dystrophy 96
C16.320.577.750 Walker-Warburg Syndrome 4
C16.320.590 Myasthenic Syndromes, Congenital 21
C16.320.600 Nail-Patella Syndrome 8
C16.320.700 Neoplastic Syndromes, Hereditary 144
C16.320.709 Oculocerebrorenal Syndrome 9
C16.320.714 Orofaciodigital Syndromes 7
C16.320.718 Osteoarthropathy, Primary Hypertrophic 127
C16.320.728 Osteochondrodysplasias 125
C16.320.737 Osteogenesis Imperfecta 106
C16.320.775 Pain Insensitivity, Congenital 10
C16.320.784 Pelger-Huet Anomaly 7
C16.320.798 Primary Immunodeficiency Diseases 48
C16.320.812 Pycnodysostosis 2
C16.320.831 Renal Tubular Transport, Inborn Errors 36
C16.320.850 Skin Diseases, Genetic 89
C16.320.925 Werner Syndrome 14
C16.320.962 Yellow Nail Syndrome

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Muscular Dystrophy, Congenital, plus Mental Retardation Disease MeSH Browser

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Myopathy, Myofibrillar, Desmin-Related Disease MeSH Browser

Myopathy, Myofibrillar, Zasp-Related Disease MeSH Browser

Oculopharyngodistal Myopathy Disease MeSH Browser

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