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Chromosome Disorders
Clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material (either a whole chromosome or a chromosome segment). (from Thompson et al., Genetics in Medicine, 5th ed, p429)
推出的年份: 2002
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:
C16.131.260, C16.320.180
MeSH 单一 ID:
D025063
进入的组:
Chromosome Disorder
Disorder, Chromosome
Disorders, Chromosome
Chromosome Abnormality Disorders
Chromosome Abnormality Disorder
Disorder, Chromosome Abnormality
Chromosomal Disorders
Chromosomal Disorder
Disorder, Chromosomal
Disorders, Chromosomal
Autosomal Chromosome Disorders
Autosomal Chromosome Disorder
Chromosome Disorder, Autosomal
Chromosome Disorders, Autosomal
早前的内容:
Chromosome Abnormalities (1964-2001)
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Drug-Induced [C16.131.042]
Abnormalities, Multiple [C16.131.077]
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Abnormalities, Radiation-Induced [C16.131.080]
Abnormalities, Severe Teratoid [C16.131.085]
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Aicardi Syndrome [C16.131.162]
Cardiovascular Abnormalities [C16.131.240]
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Chromosome Disorders [C16.131.260]
22q11 Deletion Syndrome [C16.131.260.019]
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Angelman Syndrome [C16.131.260.040]
Beckwith-Wiedemann Syndrome [C16.131.260.080]
Branchio-Oto-Renal Syndrome [C16.131.260.090]
Cri-du-Chat Syndrome [C16.131.260.190]
De Lange Syndrome [C16.131.260.210]
Down Syndrome [C16.131.260.260]
Holoprosencephaly [C16.131.260.380]
Jacobsen Distal 11q Deletion Syndrome [C16.131.260.440]
Prader-Willi Syndrome [C16.131.260.700]
Rubinstein-Taybi Syndrome [C16.131.260.790]
Sex Chromosome Disorders [C16.131.260.830]
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Silver-Russell Syndrome [C16.131.260.870]
Smith-Magenis Syndrome [C16.131.260.887]
Sotos Syndrome [C16.131.260.905]
Trisomy 13 Syndrome [C16.131.260.923]
Trisomy 18 Syndrome [C16.131.260.932]
WAGR Syndrome []
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Williams Syndrome [C16.131.260.970]
Wolf-Hirschhorn Syndrome [C16.131.260.985]
Congenital Microtia [C16.131.287]
Digestive System Abnormalities [C16.131.314]
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Eye Abnormalities [C16.131.384]
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Hernias, Diaphragmatic, Congenital [C16.131.433]
Lymphatic Abnormalities [C16.131.482]
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Musculoskeletal Abnormalities [C16.131.621]
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Nervous System Malformations [C16.131.666]
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Respiratory System Abnormalities [C16.131.740]
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Situs Inversus [C16.131.810]
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Skin Abnormalities [C16.131.831]
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Stomatognathic System Abnormalities [C16.131.850]
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Thyroid Dysgenesis [C16.131.894]
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Urogenital Abnormalities [C16.131.939]
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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]
22q11 Deletion Syndrome [C16.320.180.019]
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Angelman Syndrome [C16.320.180.040]
Beckwith-Wiedemann Syndrome [C16.320.180.080]
Branchio-Oto-Renal Syndrome [C16.320.180.090]
Cri-du-Chat Syndrome [C16.320.180.190]
De Lange Syndrome [C16.320.180.210]
Down Syndrome [C16.320.180.260]
Holoprosencephaly [C16.320.180.380]
Jacobsen Distal 11q Deletion Syndrome [C16.320.180.440]
Prader-Willi Syndrome [C16.320.180.700]
Rubinstein-Taybi Syndrome [C16.320.180.790]
Sex Chromosome Disorders [C16.320.180.830]
add_circle
Silver-Russell Syndrome [C16.320.180.870]
Smith-Magenis Syndrome [C16.320.180.887]
Sotos Syndrome [C16.320.180.905]
Trisomy 13 Syndrome [C16.320.180.923]
Trisomy 18 Syndrome [C16.320.180.932]
WAGR Syndrome []
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Williams Syndrome [C16.320.180.970]
Wolf-Hirschhorn Syndrome [C16.320.180.985]
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]
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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]
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