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Camurati-Engelmann Syndrome
An autosomal dominant form of dysplasia that is characterized by progressive thickening of diaphyseal cortex of long bones. Mutations in the gene that encodes TRANSFORMING GROWTH FACTOR BETA1 are one cause of this disorder.
推出的年份: 2007(1975)
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:
C05.116.099.708.180, C16.320.144
MeSH 单一 ID:
D003966
进入的组:
Camurati Engelmann Syndrome
Engelmann's Disease
Engelmann Disease
Camurati-Engelmann Disease
Camurati Engelmann Disease
Diaphyseal Dysplasia, Progressive
Diaphyseal Hyperostosis
Diaphyseal Hyperostoses
Hyperostoses, Diaphyseal
Hyperostosis, Diaphyseal
Diaphyseal Dysplasia 1, Progressive
Progressive Diaphyseal Dysplasia
Diaphyseal Dysplasias, Progressive
Dysplasia, Progressive Diaphyseal
Dysplasias, Progressive Diaphyseal
All MeSH Categories
Diseases Category
Musculoskeletal Diseases [C05]
Bone Diseases [C05.116]
Bone Diseases, Developmental [C05.116.099]
Osteochondrodysplasias [C05.116.099.708]
Achondroplasia [C05.116.099.708.017]
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Acquired Hyperostosis Syndrome [C05.116.099.708.025]
Camurati-Engelmann Syndrome [C05.116.099.708.180]
Chondrodysplasia Punctata [C05.116.099.708.195]
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Cleidocranial Dysplasia [C05.116.099.708.207]
Ellis-Van Creveld Syndrome [C05.116.099.708.327]
Enchondromatosis [C05.116.099.708.338]
Fibrous Dysplasia of Bone [C05.116.099.708.375]
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Hyperostosis Frontalis Interna [C05.116.099.708.486]
Hyperostosis, Cortical, Congenital [C05.116.099.708.479]
Kashin-Beck Disease [C05.116.099.708.534]
Langer-Giedion Syndrome [C05.116.099.708.582]
Osteochondroma [C05.116.099.708.670]
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Osteogenesis Imperfecta [C05.116.099.708.685]
Osteosclerosis [C05.116.099.708.702]
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Pycnodysostosis [C05.116.099.708.779]
Short Rib-Polydactyly Syndrome [C05.116.099.708.857]
Slipped Capital Femoral Epiphyses [C05.116.099.708.928]
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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