Hyperlipidemia, Familial Combined

MeSH 搜索器

Hyperlipidemia, Familial Combined

A type of familial lipid metabolism disorder characterized by a variable pattern of elevated plasma CHOLESTEROL and/or TRIGLYCERIDES. Multiple genes on different chromosomes may be involved, such as the major late transcription factor (UPSTREAM STIMULATORY FACTORS) on CHROMOSOME 1.

推出的年份: 1980

树号: C16.320.565.398.450, C18.452.584.500.500.438, C18.452.584.563.450, C18.452.648.398.450

MeSH 单一 ID: D006950

进入的组:

Combined Hyperlipidemia, Familial
Combined Hyperlipidemias, Familial
Familial Combined Hyperlipidemias
Hyperlipidemias, Familial Combined
Familial Combined Hyperlipidemia
Hyperlipidemia, Multiple Lipoprotein-Type
Hyperlipidemia, Multiple Lipoprotein Type
Hyperlipidemias, Multiple Lipoprotein-Type
Lipoprotein-Type Hyperlipidemia, Multiple
Lipoprotein-Type Hyperlipidemias, Multiple
Multiple Lipoprotein-Type Hyperlipidemia
Multiple Lipoprotein-Type Hyperlipidemias

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]
        
        Barth Syndrome [C16.320.565.398.224]
        
        Hyperlipidemia, Familial Combined [C16.320.565.398.450]
        
        Hyperlipoproteinemia Type I [C16.320.565.398.465]
        
        Hyperlipoproteinemia Type II [C16.320.565.398.481] add_circle
        
        Hyperlipoproteinemia Type III [C16.320.565.398.483]
        
        Hyperlipoproteinemia Type IV [C16.320.565.398.487]
        
        Hyperlipoproteinemia Type V [C16.320.565.398.493]
        
        Hypolipoproteinemias [C16.320.565.398.500] add_circle
        
        Lipidoses [C16.320.565.398.641] add_circle
        
        Lipodystrophy, Congenital Generalized [C16.320.565.398.745]
        
        Smith-Lemli-Opitz Syndrome [C16.320.565.398.850]
        
        Xanthomatosis, Cerebrotendinous [C16.320.565.398.925]

All MeSH Categories
- Diseases Category
  - Nutritional and Metabolic Diseases [C18]
    - Metabolic Diseases [C18.452]
      - Lipid Metabolism Disorders [C18.452.584]
        
        Dyslipidemias [C18.452.584.500]
        
        Hyperlipidemias [C18.452.584.500.500]
        
        Hypercholesterolemia [C18.452.584.500.500.396]
        
        Hyperlipidemia, Familial Combined [C18.452.584.500.500.438]
        
        Hyperlipoproteinemias [C18.452.584.500.500.644] add_circle
        
        Hypertriglyceridemia [C18.452.584.500.500.851] add_circle

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]
        
        Barth Syndrome [C18.452.584.563.224]
        
        Hyperlipidemia, Familial Combined [C18.452.584.563.450]
        
        Hyperlipoproteinemia Type I [C18.452.584.563.465]
        
        Hyperlipoproteinemia Type II [C18.452.584.563.481] add_circle
        
        Hyperlipoproteinemia Type III [C18.452.584.563.483]
        
        Hyperlipoproteinemia Type IV [C18.452.584.563.487]
        
        Hyperlipoproteinemia Type V [C18.452.584.563.493]
        
        Hypobetalipoproteinemia, Familial, Apolipoprotein B [C18.452.584.563.497]
        
        Hypolipoproteinemias [C18.452.584.563.500] add_circle
        
        Lipidoses [C18.452.584.563.641] add_circle
        
        Lipodystrophy, Congenital Generalized [C18.452.584.563.745]
        
        Lipodystrophy, Familial Partial [C18.452.584.563.798]
        
        Shwachman-Diamond Syndrome [C18.452.584.563.824]
        
        Smith-Lemli-Opitz Syndrome [C18.452.584.563.850]
        
        Xanthomatosis, Cerebrotendinous [C18.452.584.563.925]

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]
        
        Barth Syndrome [C18.452.648.398.224]
        
        Hyperlipidemia, Familial Combined [C18.452.648.398.450]
        
        Hyperlipoproteinemia Type I [C18.452.648.398.465]
        
        Hyperlipoproteinemia Type II [C18.452.648.398.481] add_circle
        
        Hyperlipoproteinemia Type III [C18.452.648.398.483]
        
        Hyperlipoproteinemia Type IV [C18.452.648.398.487]
        
        Hyperlipoproteinemia Type V [C18.452.648.398.493]
        
        Hypolipoproteinemias [C18.452.648.398.500] add_circle
        
        Lipidoses [C18.452.648.398.641] add_circle
        
        Lipodystrophy, Congenital Generalized [C18.452.648.398.745]
        
        Smith-Lemli-Opitz Syndrome [C18.452.648.398.850]
        
        Xanthomatosis, Cerebrotendinous [C18.452.648.398.925]

Like

分享书签

0 0 0 0 0 0 0

MeSH 搜索器

Hyperlipidemia, Familial Combined

副标题

留言 (0)