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Cherubism
A fibro-osseous hereditary disease of the jaws. The swollen jaws and raised eyes give a cherubic appearance; multiple radiolucencies are evident upon radiographic examination.
推出的年份: 1965
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:
C05.116.099.708.375.199, C05.500.174, C07.320.173, C16.131.621.207.540.170, C16.320.170
MeSH 单一 ID:
D002636
进入的组:
Familial Fibrous Dysplasia of Jaw
Familial Multilocular Cystic Disease of the Jaws
Familial Benign Giant-Cell Tumor of the Jaw
All MeSH Categories
Diseases Category
Musculoskeletal Diseases [C05]
Bone Diseases [C05.116]
Bone Diseases, Developmental [C05.116.099]
Osteochondrodysplasias [C05.116.099.708]
Fibrous Dysplasia of Bone [C05.116.099.708.375]
Cherubism [C05.116.099.708.375.199]
Craniofacial Fibrous Dysplasia [C05.116.099.708.375.286]
Fibrous Dysplasia, Monostotic [C05.116.099.708.375.372]
Fibrous Dysplasia, Polyostotic [C05.116.099.708.375.381]
All MeSH Categories
Diseases Category
Musculoskeletal Diseases [C05]
Jaw Diseases [C05.500]
Bisphosphonate-Associated Osteonecrosis of the Jaw [C05.500.086]
Cherubism [C05.500.174]
Granuloma, Giant Cell [C05.500.368]
Jaw Abnormalities [C05.500.460]
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Jaw Cysts [C05.500.470]
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Jaw Neoplasms [C05.500.499]
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Jaw, Edentulous [C05.500.480]
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Mandibular Diseases [C05.500.607]
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Maxillary Diseases [C05.500.693]
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All MeSH Categories
Diseases Category
Stomatognathic Diseases [C07]
Jaw Diseases [C07.320]
Bisphosphonate-Associated Osteonecrosis of the Jaw [C07.320.086]
Cherubism [C07.320.173]
Granuloma, Giant Cell [C07.320.391]
Jaw Abnormalities [C07.320.440]
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Jaw Cysts [C07.320.450]
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Jaw Neoplasms [C07.320.515]
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Jaw, Edentulous [C07.320.550]
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Mandibular Diseases [C07.320.610]
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Maxillary Diseases [C07.320.660]
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Periapical Diseases [C07.320.830]
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All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Musculoskeletal Abnormalities [C16.131.621]
Craniofacial Abnormalities [C16.131.621.207]
Maxillofacial Abnormalities [C16.131.621.207.540]
Cherubism [C16.131.621.207.540.170]
Dentofacial Deformities [C16.131.621.207.540.315]
Jaw Abnormalities [C16.131.621.207.540.460]
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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]
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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]
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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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