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Renal Tubular Transport, Inborn Errors
Genetic defects in the selective or non-selective transport functions of the KIDNEY TUBULES.
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:
C12.050.351.968.419.815, C12.200.777.419.815, C12.950.419.815, C16.320.565.893, C16.320.831, C18.452.648.893
MeSH 单一 ID:
D015499
进入的组:
Renal Tubular Transport Errors
Renal Tubular Transport, Inborn Error
Kidney Tubular Transport, Inborn Error
Kidney Tubular Transport, Inborn Errors
All MeSH Categories
Diseases Category
Urogenital Diseases [C12]
Female Urogenital Diseases and Pregnancy Complications [C12.050]
Female Urogenital Diseases [C12.050.351]
Urologic Diseases [C12.050.351.968]
Kidney Diseases [C12.050.351.968.419]
AIDS-Associated Nephropathy [C12.050.351.968.419.050]
Anuria [C12.050.351.968.419.078]
Chronic Kidney Disease-Mineral and Bone Disorder [C12.050.351.968.419.795]
Diabetes Insipidus [C12.050.351.968.419.135]
add_circle
Diabetic Nephropathies [C12.050.351.968.419.192]
Hepatorenal Syndrome [C12.050.351.968.419.291]
Hydronephrosis [C12.050.351.968.419.307]
add_circle
Hyperoxaluria [C12.050.351.968.419.313]
add_circle
Hypertension, Renal [C12.050.351.968.419.331]
add_circle
Kidney Cortex Necrosis [C12.050.351.968.419.393]
Kidney Diseases, Cystic [C12.050.351.968.419.403]
add_circle
Kidney Neoplasms [C12.050.351.968.419.473]
add_circle
Kidney Papillary Necrosis [C12.050.351.968.419.493]
Nephritis [C12.050.351.968.419.570]
add_circle
Nephrocalcinosis [C12.050.351.968.419.590]
Nephrolithiasis [C12.050.351.968.419.600]
add_circle
Nephrosclerosis [C12.050.351.968.419.610]
Nephrosis [C12.050.351.968.419.630]
add_circle
Perinephritis [C12.050.351.968.419.685]
Renal Artery Obstruction [C12.050.351.968.419.775]
Renal Insufficiency [C12.050.351.968.419.780]
add_circle
Renal Nutcracker Syndrome [C12.050.351.968.419.787]
Renal Tubular Transport, Inborn Errors [C12.050.351.968.419.815]
Acidosis, Renal Tubular [C12.050.351.968.419.815.093]
Bartter Syndrome [C12.050.351.968.419.815.279]
Dent Disease [C12.050.351.968.419.815.364]
Fanconi Syndrome [C12.050.351.968.419.815.450]
Gitelman Syndrome [C12.050.351.968.419.815.491]
Glycosuria, Renal [C12.050.351.968.419.815.532]
Hypophosphatemia, Familial [C12.050.351.968.419.815.647]
add_circle
Liddle Syndrome [C12.050.351.968.419.815.683]
Oculocerebrorenal Syndrome [C12.050.351.968.419.815.720]
Pseudohypoaldosteronism [C12.050.351.968.419.815.770]
Renal Aminoacidurias [C12.050.351.968.419.815.885]
add_circle
Tuberculosis, Renal [C12.050.351.968.419.912]
Uremia [C12.050.351.968.419.936]
add_circle
Zellweger Syndrome [C12.050.351.968.419.978]
All MeSH Categories
Diseases Category
Urogenital Diseases [C12]
Male Urogenital Diseases [C12.200]
Urologic Diseases [C12.200.777]
Kidney Diseases [C12.200.777.419]
AIDS-Associated Nephropathy [C12.200.777.419.050]
Anuria [C12.200.777.419.078]
Chronic Kidney Disease-Mineral and Bone Disorder [C12.200.777.419.080]
Diabetes Insipidus [C12.200.777.419.135]
add_circle
Diabetic Nephropathies [C12.200.777.419.192]
Hepatorenal Syndrome [C12.200.777.419.291]
Hydronephrosis [C12.200.777.419.307]
add_circle
Hyperoxaluria [C12.200.777.419.313]
add_circle
Hypertension, Renal [C12.200.777.419.331]
add_circle
Kidney Cortex Necrosis [C12.200.777.419.393]
Kidney Diseases, Cystic [C12.200.777.419.403]
add_circle
Kidney Neoplasms [C12.200.777.419.473]
add_circle
Kidney Papillary Necrosis [C12.200.777.419.493]
Nephritis [C12.200.777.419.570]
add_circle
Nephrocalcinosis [C12.200.777.419.590]
Nephrolithiasis [C12.200.777.419.600]
add_circle
Nephrosclerosis [C12.200.777.419.610]
Nephrosis [C12.200.777.419.630]
add_circle
Perinephritis [C12.200.777.419.685]
Renal Artery Obstruction [C12.200.777.419.775]
Renal Insufficiency [C12.200.777.419.780]
add_circle
Renal Nutcracker Syndrome [C12.200.777.419.787]
Renal Tubular Transport, Inborn Errors [C12.200.777.419.815]
Acidosis, Renal Tubular [C12.200.777.419.815.093]
Bartter Syndrome [C12.200.777.419.815.279]
Dent Disease [C12.200.777.419.815.364]
Fanconi Syndrome [C12.200.777.419.815.450]
Gitelman Syndrome [C12.200.777.419.815.491]
Glycosuria, Renal [C12.200.777.419.815.532]
Hypophosphatemia, Familial [C12.200.777.419.815.647]
add_circle
Liddle Syndrome [C12.200.777.419.815.683]
Oculocerebrorenal Syndrome [C12.200.777.419.815.720]
Pseudohypoaldosteronism [C12.200.777.419.815.770]
Renal Aminoacidurias [C12.200.777.419.815.885]
add_circle
Tuberculosis, Renal [C12.200.777.419.912]
Uremia [C12.200.777.419.936]
add_circle
Zellweger Syndrome [C12.200.777.419.978]
All MeSH Categories
Diseases Category
Urogenital Diseases [C12]
Urologic Diseases [C12.950]
Kidney Diseases [C12.950.419]
AIDS-Associated Nephropathy [C12.950.419.050]
Anuria [C12.950.419.078]
Chronic Kidney Disease-Mineral and Bone Disorder [C12.950.419.795]
Diabetes Insipidus [C12.950.419.135]
add_circle
Diabetic Nephropathies [C12.950.419.192]
Hepatorenal Syndrome [C12.950.419.291]
Hydronephrosis [C12.950.419.307]
add_circle
Hyperoxaluria [C12.950.419.313]
add_circle
Hypertension, Renal [C12.950.419.331]
add_circle
Kidney Cortex Necrosis [C12.950.419.393]
Kidney Diseases, Cystic [C12.950.419.403]
add_circle
Kidney Neoplasms [C12.950.419.473]
add_circle
Kidney Papillary Necrosis [C12.950.419.493]
Nephritis [C12.950.419.570]
add_circle
Nephrocalcinosis [C12.950.419.590]
Nephrolithiasis [C12.950.419.600]
add_circle
Nephrosclerosis [C12.950.419.610]
Nephrosis [C12.950.419.630]
add_circle
Perinephritis [C12.950.419.685]
Renal Artery Obstruction [C12.950.419.775]
Renal Insufficiency [C12.950.419.780]
add_circle
Renal Nutcracker Syndrome [C12.950.419.787]
Renal Tubular Transport, Inborn Errors [C12.950.419.815]
Acidosis, Renal Tubular [C12.950.419.815.093]
Bartter Syndrome [C12.950.419.815.279]
Dent Disease [C12.950.419.815.364]
Fanconi Syndrome [C12.950.419.815.450]
Gitelman Syndrome [C12.950.419.815.491]
Glycosuria, Renal [C12.950.419.815.532]
Hypophosphatemia, Familial [C12.950.419.815.647]
add_circle
Liddle Syndrome [C12.950.419.815.683]
Oculocerebrorenal Syndrome [C12.950.419.815.720]
Pseudohypoaldosteronism [C12.950.419.815.770]
Renal Aminoacidurias [C12.950.419.815.885]
add_circle
Tuberculosis, Renal [C12.950.419.912]
Uremia [C12.950.419.936]
add_circle
Zellweger Syndrome [C12.950.419.978]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Amino Acid Metabolism, Inborn Errors [C16.320.565.100]
add_circle
Amino Acid Transport Disorders, Inborn [C16.320.565.151]
add_circle
Amyloidosis, Familial [C16.320.565.176]
add_circle
Brain Diseases, Metabolic, Inborn [C16.320.565.189]
add_circle
Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
add_circle
Cytochrome-c Oxidase Deficiency [C16.320.565.240]
Hyperbilirubinemia, Hereditary [C16.320.565.300]
add_circle
Lipid Metabolism, Inborn Errors [C16.320.565.398]
add_circle
Lysosomal Storage Diseases [C16.320.565.595]
add_circle
Metal Metabolism, Inborn Errors [C16.320.565.618]
add_circle
Peroxisomal Disorders [C16.320.565.663]
add_circle
Progeria [C16.320.565.753]
Purine-Pyrimidine Metabolism, Inborn Errors [C16.320.565.798]
add_circle
Renal Tubular Transport, Inborn Errors [C16.320.565.893]
Steroid Metabolism, Inborn Errors [C16.320.565.925]
add_circle
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]
add_circle
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]
All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Metabolism, Inborn Errors [C18.452.648]
Amino Acid Metabolism, Inborn Errors [C18.452.648.100]
add_circle
Amino Acid Transport Disorders, Inborn [C18.452.648.151]
add_circle
Amyloidosis, Familial [C18.452.648.176]
add_circle
Brain Diseases, Metabolic, Inborn [C18.452.648.189]
add_circle
Carbohydrate Metabolism, Inborn Errors [C18.452.648.202]
add_circle
Hyperbilirubinemia, Hereditary [C18.452.648.300]
add_circle
Lipid Metabolism, Inborn Errors [C18.452.648.398]
add_circle
Lysosomal Storage Diseases [C18.452.648.595]
add_circle
Metal Metabolism, Inborn Errors [C18.452.648.618]
add_circle
Peroxisomal Disorders [C18.452.648.663]
add_circle
Progeria [C18.452.648.753]
Purine-Pyrimidine Metabolism, Inborn Errors [C18.452.648.798]
add_circle
Renal Tubular Transport, Inborn Errors [C18.452.648.893]
Steroid Metabolism, Inborn Errors [C18.452.648.925]
add_circle
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