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Lysosomal Storage Diseases
Inborn errors of metabolism characterized by defects in specific lysosomal hydrolases and resulting in intracellular accumulation of unmetabolized substrates.
推出的年份: 1992
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:
C16.320.565.595, C18.452.648.595
MeSH 单一 ID:
D016464
进入的组:
Disease, Lysosomal Storage
Diseases, Lysosomal Storage
Lysosomal Storage Disease
Lysosomal Enzyme Disorders
Disorder, Lysosomal Enzyme
Disorders, Lysosomal Enzyme
Enzyme Disorder, Lysosomal
Enzyme Disorders, Lysosomal
Lysosomal Enzyme Disorder
早前的内容:
Metabolism, Inborn Errors (1972-1991)
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]
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Amyloidosis, Familial [C16.320.565.176]
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Brain Diseases, Metabolic, Inborn [C16.320.565.189]
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Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
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Cytochrome-c Oxidase Deficiency [C16.320.565.240]
Hyperbilirubinemia, Hereditary [C16.320.565.300]
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Lipid Metabolism, Inborn Errors [C16.320.565.398]
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Lysosomal Storage Diseases [C16.320.565.595]
Aspartylglucosaminuria [C16.320.565.595.100]
Cholesterol Ester Storage Disease [C16.320.565.595.201]
add_circle
Cystinosis [C16.320.565.595.377]
Lysosomal Storage Diseases, Nervous System [C16.320.565.595.554]
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Mannosidase Deficiency Diseases [C16.320.565.595.577]
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Mucopolysaccharidoses [C16.320.565.595.600]
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Pycnodysostosis [C16.320.565.595.800]
Metal Metabolism, Inborn Errors [C16.320.565.618]
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Peroxisomal Disorders [C16.320.565.663]
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Progeria [C16.320.565.753]
Purine-Pyrimidine Metabolism, Inborn Errors [C16.320.565.798]
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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]
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]
Aspartylglucosaminuria [C18.452.648.595.100]
Cholesterol Ester Storage Disease [C18.452.648.595.201]
add_circle
Cystinosis [C18.452.648.595.377]
Lysosomal Storage Diseases, Nervous System [C18.452.648.595.554]
add_circle
Mannosidase Deficiency Diseases [C18.452.648.595.577]
add_circle
Mucopolysaccharidoses [C18.452.648.595.600]
add_circle
Pycnodysostosis [C18.452.648.595.800]
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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