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MeSH 搜索器

Sulfatidosis

A group of inherited metabolic disorders characterized by the intralysosomal accumulation of sulfur-containing lipids (SULFATIDES), including SULFOGLYCOSPHINGOLIPIDS normally found in the MYELIN SHEATH of the brain. These disorders are caused by defective degradative enzymes leading to substrate accumulation (or storage).

推出的年份: 2007

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: C10.228.140.163.100.435.825.850, C16.320.565.189.435.825.850, C16.320.565.398.641.803.925, C16.320.565.595.554.825.850, C18.452.132.100.435.825.850, C18.452.584.563.641.803.925, C18.452.648.189.435.825.850, C18.452.648.398.641.803.925, C18.452.648.595.554.825.850

MeSH 单一 ID: D052516

进入的组:

Sulfatidoses

All MeSH Categories
- Diseases Category
  - Nervous System Diseases [C10]
    - Central Nervous System Diseases [C10.228]
      - Brain Diseases [C10.228.140]
        
        Brain Diseases, Metabolic [C10.228.140.163]
        
        Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
        
        Lysosomal Storage Diseases, Nervous System [C10.228.140.163.100.435]
        
        Sphingolipidoses [C10.228.140.163.100.435.825]
        
        Fabry Disease [C10.228.140.163.100.435.825.200]
        
        Farber Lipogranulomatosis [C10.228.140.163.100.435.825.250]
        
        Gangliosidoses [C10.228.140.163.100.435.825.300] add_circle
        
        Gaucher Disease [C10.228.140.163.100.435.825.400]
        
        Leukodystrophy, Globoid Cell [C10.228.140.163.100.435.825.590]
        
        Niemann-Pick Diseases [C10.228.140.163.100.435.825.700] add_circle
        
        Sea-Blue Histiocyte Syndrome [C10.228.140.163.100.435.825.775]
        
        Sulfatidosis [C10.228.140.163.100.435.825.850]
        
        Leukodystrophy, Metachromatic [C10.228.140.163.100.435.825.850.500]
        
        Multiple Sulfatase Deficiency Disease [C10.228.140.163.100.435.825.850.750]

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Genetic Diseases, Inborn [C16.320]
      - Metabolism, Inborn Errors [C16.320.565]
        
        Brain Diseases, Metabolic, Inborn [C16.320.565.189]
        
        Lysosomal Storage Diseases, Nervous System [C16.320.565.189.435]
        
        Sphingolipidoses [C16.320.565.189.435.825]
        
        Fabry Disease [C16.320.565.189.435.825.200]
        
        Farber Lipogranulomatosis [C16.320.565.189.435.825.250]
        
        Gangliosidoses [C16.320.565.189.435.825.300] add_circle
        
        Gaucher Disease [C16.320.565.189.435.825.400]
        
        Leukodystrophy, Globoid Cell [C16.320.565.189.435.825.590]
        
        Niemann-Pick Diseases [C16.320.565.189.435.825.700] add_circle
        
        Sea-Blue Histiocyte Syndrome [C16.320.565.189.435.825.775]
        
        Sulfatidosis [C16.320.565.189.435.825.850]
        
        Leukodystrophy, Metachromatic [C16.320.565.189.435.825.850.500]
        
        Multiple Sulfatase Deficiency Disease [C16.320.565.189.435.825.850.750]

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Genetic Diseases, Inborn [C16.320]
      - Metabolism, Inborn Errors [C16.320.565]
        
        Lipid Metabolism, Inborn Errors [C16.320.565.398]
        
        Lipidoses [C16.320.565.398.641]
        
        Sphingolipidoses [C16.320.565.398.641.803]
        
        Fabry Disease [C16.320.565.398.641.803.300]
        
        Farber Lipogranulomatosis [C16.320.565.398.641.803.325]
        
        Gangliosidoses [C16.320.565.398.641.803.350] add_circle
        
        Gaucher Disease [C16.320.565.398.641.803.441]
        
        Leukodystrophy, Globoid Cell [C16.320.565.398.641.803.585]
        
        Niemann-Pick Diseases [C16.320.565.398.641.803.730] add_circle
        
        Sea-Blue Histiocyte Syndrome [C16.320.565.398.641.803.850]
        
        Sulfatidosis [C16.320.565.398.641.803.925]
        
        Leukodystrophy, Metachromatic [C16.320.565.398.641.803.925.500]
        
        Multiple Sulfatase Deficiency Disease [C16.320.565.398.641.803.925.750]

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Genetic Diseases, Inborn [C16.320]
      - Metabolism, Inborn Errors [C16.320.565]
        
        Lysosomal Storage Diseases [C16.320.565.595]
        
        Lysosomal Storage Diseases, Nervous System [C16.320.565.595.554]
        
        Sphingolipidoses [C16.320.565.595.554.825]
        
        Fabry Disease [C16.320.565.595.554.825.200]
        
        Farber Lipogranulomatosis [C16.320.565.595.554.825.250]
        
        Gangliosidoses [C16.320.565.595.554.825.300] add_circle
        
        Gaucher Disease [C16.320.565.595.554.825.400]
        
        Leukodystrophy, Globoid Cell [C16.320.565.595.554.825.590]
        
        Niemann-Pick Diseases [C16.320.565.595.554.825.700] add_circle
        
        Sea-Blue Histiocyte Syndrome [C16.320.565.595.554.825.775]
        
        Sulfatidosis [C16.320.565.595.554.825.850]
        
        Leukodystrophy, Metachromatic [C16.320.565.595.554.825.850.500]
        
        Multiple Sulfatase Deficiency Disease [C16.320.565.595.554.825.850.750]

All MeSH Categories
- Diseases Category
  - Nutritional and Metabolic Diseases [C18]
    - Metabolic Diseases [C18.452]
      - Brain Diseases, Metabolic [C18.452.132]
        
        Brain Diseases, Metabolic, Inborn [C18.452.132.100]
        
        Lysosomal Storage Diseases, Nervous System [C18.452.132.100.435]
        
        Sphingolipidoses [C18.452.132.100.435.825]
        
        Fabry Disease [C18.452.132.100.435.825.200]
        
        Farber Lipogranulomatosis [C18.452.132.100.435.825.250]
        
        Gangliosidoses [C18.452.132.100.435.825.300] add_circle
        
        Gaucher Disease [C18.452.132.100.435.825.400]
        
        Leukodystrophy, Globoid Cell [C18.452.132.100.435.825.590]
        
        Niemann-Pick Diseases [C18.452.132.100.435.825.700] add_circle
        
        Sea-Blue Histiocyte Syndrome [C18.452.132.100.435.825.775]
        
        Sulfatidosis [C18.452.132.100.435.825.850]
        
        Leukodystrophy, Metachromatic [C18.452.132.100.435.825.850.500]
        
        Multiple Sulfatase Deficiency Disease [C18.452.132.100.435.825.850.750]

All MeSH Categories
- Diseases Category
  - Nutritional and Metabolic Diseases [C18]
    - Metabolic Diseases [C18.452]
      - Lipid Metabolism Disorders [C18.452.584]
        
        Lipid Metabolism, Inborn Errors [C18.452.584.563]
        
        Lipidoses [C18.452.584.563.641]
        
        Sphingolipidoses [C18.452.584.563.641.803]
        
        Fabry Disease [C18.452.584.563.641.803.300]
        
        Farber Lipogranulomatosis [C18.452.584.563.641.803.325]
        
        Gangliosidoses [C18.452.584.563.641.803.350] add_circle
        
        Gaucher Disease [C18.452.584.563.641.803.441]
        
        Leukodystrophy, Globoid Cell [C18.452.584.563.641.803.585]
        
        Niemann-Pick Diseases [C18.452.584.563.641.803.730] add_circle
        
        Sea-Blue Histiocyte Syndrome [C18.452.584.563.641.803.850]
        
        Sulfatidosis [C18.452.584.563.641.803.925]
        
        Leukodystrophy, Metachromatic [C18.452.584.563.641.803.925.500]
        
        Multiple Sulfatase Deficiency Disease [C18.452.584.563.641.803.925.750]

All MeSH Categories
- Diseases Category
  - Nutritional and Metabolic Diseases [C18]
    - Metabolic Diseases [C18.452]
      - Metabolism, Inborn Errors [C18.452.648]
        
        Brain Diseases, Metabolic, Inborn [C18.452.648.189]
        
        Lysosomal Storage Diseases, Nervous System [C18.452.648.189.435]
        
        Sphingolipidoses [C18.452.648.189.435.825]
        
        Fabry Disease [C18.452.648.189.435.825.200]
        
        Farber Lipogranulomatosis [C18.452.648.189.435.825.250]
        
        Gangliosidoses [C18.452.648.189.435.825.300] add_circle
        
        Gaucher Disease [C18.452.648.189.435.825.400]
        
        Leukodystrophy, Globoid Cell [C18.452.648.189.435.825.590]
        
        Niemann-Pick Diseases [C18.452.648.189.435.825.700] add_circle
        
        Sea-Blue Histiocyte Syndrome [C18.452.648.189.435.825.775]
        
        Sulfatidosis [C18.452.648.189.435.825.850]
        
        Leukodystrophy, Metachromatic [C18.452.648.189.435.825.850.500]
        
        Multiple Sulfatase Deficiency Disease [C18.452.648.189.435.825.850.750]

All MeSH Categories
- Diseases Category
  - Nutritional and Metabolic Diseases [C18]
    - Metabolic Diseases [C18.452]
      - Metabolism, Inborn Errors [C18.452.648]
        
        Lipid Metabolism, Inborn Errors [C18.452.648.398]
        
        Lipidoses [C18.452.648.398.641]
        
        Sphingolipidoses [C18.452.648.398.641.803]
        
        Fabry Disease [C18.452.648.398.641.803.300]
        
        Farber Lipogranulomatosis [C18.452.648.398.641.803.325]
        
        Gangliosidoses [C18.452.648.398.641.803.350] add_circle
        
        Gaucher Disease [C18.452.648.398.641.803.441]
        
        Leukodystrophy, Globoid Cell [C18.452.648.398.641.803.585]
        
        Niemann-Pick Diseases [C18.452.648.398.641.803.730] add_circle
        
        Sea-Blue Histiocyte Syndrome [C18.452.648.398.641.803.850]
        
        Sulfatidosis [C18.452.648.398.641.803.925]
        
        Leukodystrophy, Metachromatic [C18.452.648.398.641.803.925.500]
        
        Multiple Sulfatase Deficiency Disease [C18.452.648.398.641.803.925.750]

All MeSH Categories
- Diseases Category
  - Nutritional and Metabolic Diseases [C18]
    - Metabolic Diseases [C18.452]
      - Metabolism, Inborn Errors [C18.452.648]
        
        Lysosomal Storage Diseases [C18.452.648.595]
        
        Lysosomal Storage Diseases, Nervous System [C18.452.648.595.554]
        
        Sphingolipidoses [C18.452.648.595.554.825]
        
        Fabry Disease [C18.452.648.595.554.825.200]
        
        Farber Lipogranulomatosis [C18.452.648.595.554.825.250]
        
        Gangliosidoses [C18.452.648.595.554.825.300] add_circle
        
        Gaucher Disease [C18.452.648.595.554.825.400]
        
        Leukodystrophy, Globoid Cell [C18.452.648.595.554.825.590]
        
        Niemann-Pick Diseases [C18.452.648.595.554.825.700] add_circle
        
        Sea-Blue Histiocyte Syndrome [C18.452.648.595.554.825.775]
        
        Sulfatidosis [C18.452.648.595.554.825.850]
        
        Leukodystrophy, Metachromatic [C18.452.648.595.554.825.850.500]
        
        Multiple Sulfatase Deficiency Disease [C18.452.648.595.554.825.850.750]

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