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Dwarfism
A genetic or pathological condition that is characterized by short stature and undersize. Abnormal skeletal growth usually results in an adult who is significantly below the average height.
推出的年份:
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
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:
C05.116.099.343, C16.320.240, C19.297
MeSH 单一 ID:
D004392
进入的组:
Nanism
All MeSH Categories
Diseases Category
Musculoskeletal Diseases [C05]
Bone Diseases [C05.116]
Bone Diseases, Developmental [C05.116.099]
Acro-Osteolysis [C05.116.099.052]
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Basal Cell Nevus Syndrome [C05.116.099.105]
Dwarfism [C05.116.099.343]
Achondroplasia [C05.116.099.343.110]
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Cockayne Syndrome [C05.116.099.343.250]
Congenital Hypothyroidism [C05.116.099.343.347]
Dwarfism, Pituitary [C05.116.099.343.445]
Laron Syndrome [C05.116.099.343.679]
Mulibrey Nanism [C05.116.099.343.796]
Weill-Marchesani Syndrome [C05.116.099.343.957]
Dysostoses [C05.116.099.370]
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Funnel Chest [C05.116.099.386]
Gigantism [C05.116.099.492]
Leg Length Inequality [C05.116.099.655]
Marfan Syndrome [C05.116.099.674]
Osteochondrodysplasias [C05.116.099.708]
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Osteolysis, Essential [C05.116.099.736]
Pectus Carinatum [C05.116.099.739]
Platybasia [C05.116.099.742]
Proteus Syndrome [C05.116.099.750]
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]
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Anemia, Hypoplastic, Congenital [C16.320.077]
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Ataxia Telangiectasia [C16.320.080]
Autoimmune Lymphoproliferative Syndrome [C16.320.089]
Blood Coagulation Disorders, Inherited [C16.320.099]
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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]
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Ciliopathies [C16.320.184]
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Costello Syndrome [C16.320.188]
Cystic Fibrosis [C16.320.190]
Donohue Syndrome [C16.320.215]
Dwarfism [C16.320.240]
Achondroplasia [C16.320.240.500]
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Cockayne Syndrome [C16.320.240.562]
Congenital Hypothyroidism [C16.320.240.625]
Laron Syndrome [C16.320.240.750]
Mulibrey Nanism [C16.320.240.875]
Silver-Russell Syndrome [C16.320.240.937]
Eye Diseases, Hereditary [C16.320.290]
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Familial Multiple Lipomatosis [C16.320.298]
Frasier Syndrome [C16.320.306]
GATA2 Deficiency [C16.320.314]
Genetic Diseases, X-Linked [C16.320.322]
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Genetic Diseases, Y-Linked [C16.320.338]
Hajdu-Cheney Syndrome [C16.320.355]
Hemoglobinopathies [C16.320.365]
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Hereditary Autoinflammatory Diseases [C16.320.382]
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Heredodegenerative Disorders, Nervous System [C16.320.400]
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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]
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Lennox Gastaut Syndrome [C16.320.495]
Loeys-Dietz Syndrome [C16.320.510]
Marfan Syndrome [C16.320.540]
Metabolism, Inborn Errors [C16.320.565]
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Muscular Dystrophies [C16.320.577]
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Myasthenic Syndromes, Congenital [C16.320.590]
Nail-Patella Syndrome [C16.320.600]
Neoplastic Syndromes, Hereditary [C16.320.700]
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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]
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Pycnodysostosis [C16.320.565.595.800]
Renal Tubular Transport, Inborn Errors [C16.320.565.893]
Skin Diseases, Genetic [C16.320.850]
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Werner Syndrome [C16.320.925]
Yellow Nail Syndrome [C16.320.962]
All MeSH Categories
Diseases Category
Endocrine System Diseases [C19]
Adrenal Gland Diseases [C19.053]
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Bone Diseases, Endocrine [C19.149]
Diabetes Mellitus [C19.246]
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Dwarfism [C19.297]
Congenital Hypothyroidism [C19.297.155]
Dwarfism, Pituitary [C19.297.312]
Laron Syndrome [C19.297.656]
Endocrine Gland Neoplasms [C19.344]
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Gonadal Disorders [C19.391]
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Parathyroid Diseases [C19.642]
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Pituitary Diseases [C19.700]
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Polyendocrinopathies, Autoimmune [C19.787]
Thyroid Diseases [C19.874]
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Tuberculosis, Endocrine [C19.927]
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