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Carbohydrate Metabolism, Inborn Errors
Dysfunctions of CARBOHYDRATE METABOLISM resulting from inborn genetic mutations that are inherited or acquired in utero.
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:
C16.320.565.202, C18.452.648.202
MeSH 单一 ID:
D002239
进入的组:
Carbohydrate Metabolism, Inborn Error
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]
Congenital Disorders of Glycosylation [C16.320.565.202.125]
Fructose Metabolism, Inborn Errors [C16.320.565.202.251]
add_circle
Fucosidosis [C16.320.565.202.303]
Galactosemias [C16.320.565.202.355]
Glucosephosphate Dehydrogenase Deficiency [C16.320.565.202.402]
Glycogen Storage Disease [C16.320.565.202.449]
add_circle
Hyperoxaluria, Primary [C16.320.565.202.460]
Lactose Intolerance [C16.320.565.202.589]
Mannosidase Deficiency Diseases [C16.320.565.202.607]
add_circle
Mucolipidoses [C16.320.565.202.670]
Mucopolysaccharidoses [C16.320.565.202.715]
add_circle
Multiple Carboxylase Deficiency [C16.320.565.202.720]
add_circle
Pyruvate Metabolism, Inborn Errors [C16.320.565.202.810]
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
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]
Congenital Disorders of Glycosylation [C18.452.648.202.125]
Fructose Metabolism, Inborn Errors [C18.452.648.202.251]
add_circle
Fucosidosis [C18.452.648.202.303]
Galactosemias [C18.452.648.202.355]
Glucosephosphate Dehydrogenase Deficiency [C18.452.648.202.402]
Glycogen Storage Disease [C18.452.648.202.449]
add_circle
Hyperoxaluria, Primary [C18.452.648.202.460]
Lactose Intolerance [C18.452.648.202.589]
Mannosidase Deficiency Diseases [C18.452.648.202.607]
add_circle
Mucolipidoses [C18.452.648.202.670]
Mucopolysaccharidoses [C18.452.648.202.715]
add_circle
Multiple Carboxylase Deficiency [C18.452.648.202.720]
add_circle
Pyruvate Metabolism, Inborn Errors [C18.452.648.202.810]
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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