×
Close
註冊
登入
主页
用户
博客
照片
视频
医学图书S馆
医学图书M馆
医学图书D馆
医学术语
群组
活动
用户工具
用户指南
问答
谁看过我
反馈
语言
English
中文
推广
所有
MeSH descriptor
Mesh Subheading
Mesh Supplementary Concept
Mesh Pharmacological Action
search
搜索
清除所有
MeSH 搜索器
AND
OR
加入MeSH搜索引擎
搜索PubMed论文列
清除所有
Muscular Dystrophies
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.
推出的年份: 2000(1966)
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
congenital
diagnosis
diagnostic imaging
diet therapy
drug therapy
economics
embryology
enzymology
epidemiology
ethnology
etiology
genetics
history
immunology
metabolism
microbiology
mortality
nursing
parasitology
pathology
physiopathology
prevention and control
psychology
radiotherapy
rehabilitation
surgery
therapy
urine
veterinary
virology
树号:
C05.651.534.500, C10.668.491.175.500, C16.320.577
MeSH 单一 ID:
D009136
进入的组:
Myodystrophica
Myodystrophicas
Myodystrophy
Myodystrophies
Muscular Dystrophy
Dystrophies, Muscular
Dystrophy, Muscular
All MeSH Categories
Diseases Category
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]
add_circle
Muscular Dystrophy, Duchenne [C05.651.534.500.300]
Muscular Dystrophy, Emery-Dreifuss [C05.651.534.500.350]
add_circle
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]
All MeSH Categories
Diseases Category
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]
Glycogen Storage Disease Type VII [C10.668.491.175.500.112]
Muscular Dystrophies, Limb-Girdle [C10.668.491.175.500.149]
add_circle
Muscular Dystrophy, Duchenne [C10.668.491.175.500.300]
Muscular Dystrophy, Emery-Dreifuss [C10.668.491.175.500.350]
add_circle
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]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Adrenal Hyperplasia, Congenital [C16.320.033]
Alagille Syndrome [C16.320.051]
alpha 1-Antitrypsin Deficiency [C16.320.060]
Anemia, Hemolytic, Congenital [C16.320.070]
add_circle
Anemia, Hypoplastic, Congenital [C16.320.077]
add_circle
Ataxia Telangiectasia [C16.320.080]
Autoimmune Lymphoproliferative Syndrome [C16.320.089]
Blood Coagulation Disorders, Inherited [C16.320.099]
add_circle
Brugada Syndrome [C16.320.100]
CADASIL [C16.320.129]
Camurati-Engelmann Syndrome [C16.320.144]
Cardiomyopathy, Hypertrophic, Familial [C16.320.160]
CHARGE Syndrome [C16.320.165]
Cherubism [C16.320.170]
Chromosome Disorders [C16.320.180]
add_circle
Ciliopathies [C16.320.184]
add_circle
Costello Syndrome [C16.320.188]
Cystic Fibrosis [C16.320.190]
Donohue Syndrome [C16.320.215]
Dwarfism [C16.320.240]
add_circle
Eye Diseases, Hereditary [C16.320.290]
add_circle
Familial Multiple Lipomatosis [C16.320.298]
Frasier Syndrome [C16.320.306]
GATA2 Deficiency [C16.320.314]
Genetic Diseases, X-Linked [C16.320.322]
add_circle
Genetic Diseases, Y-Linked [C16.320.338]
Hajdu-Cheney Syndrome [C16.320.355]
Hemoglobinopathies [C16.320.365]
add_circle
Hereditary Autoinflammatory Diseases [C16.320.382]
add_circle
Heredodegenerative Disorders, Nervous System [C16.320.400]
add_circle
Hyper-IgM Immunodeficiency Syndrome [C16.320.413]
Hyperthyroxinemia, Familial Dysalbuminemic [C16.320.427]
Kallmann Syndrome [C16.320.467]
Kartagener Syndrome [C16.320.184.500.531]
Laminopathies [C16.320.488]
add_circle
Lennox Gastaut Syndrome [C16.320.495]
Loeys-Dietz Syndrome [C16.320.510]
Marfan Syndrome [C16.320.540]
Metabolism, Inborn Errors [C16.320.565]
add_circle
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]
add_circle
Muscular Dystrophy, Duchenne [C16.320.577.300]
Muscular Dystrophy, Emery-Dreifuss [C16.320.577.350]
add_circle
Muscular Dystrophy, Facioscapulohumeral [C16.320.577.400]
Muscular Dystrophy, Oculopharyngeal [C16.320.577.450]
Myotonic Dystrophy [C16.320.577.500]
Walker-Warburg Syndrome [C16.320.577.750]
Myasthenic Syndromes, Congenital [C16.320.590]
Nail-Patella Syndrome [C16.320.600]
Neoplastic Syndromes, Hereditary [C16.320.700]
add_circle
Oculocerebrorenal Syndrome [C16.320.322.750]
Orofaciodigital Syndromes [C16.320.180.830.670]
Osteoarthropathy, Primary Hypertrophic [C16.320.718]
Osteochondrodysplasias [C16.320.728]
Osteogenesis Imperfecta [C16.320.737]
Pain Insensitivity, Congenital [C16.320.775]
Pelger-Huet Anomaly [C16.320.784]
Primary Immunodeficiency Diseases [C16.320.798]
add_circle
Pycnodysostosis [C16.320.565.595.800]
Renal Tubular Transport, Inborn Errors [C16.320.565.893]
Skin Diseases, Genetic [C16.320.850]
add_circle
Werner Syndrome [C16.320.925]
Yellow Nail Syndrome [C16.320.962]
thumb_up
Like
share
分享
favorite
书签
0
0
0
0
0
0
0
留言 (
0
)
gif
登入或註冊以發表你的留言
Modal title
×
Modal title
×
分享
登入
Global News and Health Forum
Join Now!
馬上登入
記住我
忘記密碼?
或者使用
Linkedin
留言 (0)