Homozygous Familial Hypercholesterolemia

MeSH 搜索器

Homozygous Familial Hypercholesterolemia

A rare inherited genetic disorder, one form of HYPERLIPOPROTEINEMIA TYPE II, characterized by high level of LOW-DENSITY LIPOPROTEIN (LDL) which if not treated could elevate the chance of heart attack at an early age.

推出的年份: 2022

树号: C16.320.565.398.481.500, C18.452.584.500.500.644.475.500, C18.452.584.563.481.500, C18.452.648.398.481.500

MeSH 单一 ID: D000090542

进入的组:

Hypercholesterolemias, Homozygous Familial
HoFH
Autosomal Recessive Hypercholesterolemia
Autosomal Recessive Hypercholesterolemias
Hypercholesterolemias, Autosomal Recessive
Recessive Hypercholesterolemia, Autosomal
Recessive Hypercholesterolemias, Autosomal

早前的内容:

Hypercholesterolemia (1966-2021) / Hyperlipidemia/familial & genetic (1966-2021)

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]
        
        Hyperlipoproteinemia Type II [C16.320.565.398.481]
        
        Homozygous Familial Hypercholesterolemia [C16.320.565.398.481.500]

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]
        
        Hyperlipoproteinemias [C18.452.584.500.500.644]
        
        Hyperlipoproteinemia Type II [C18.452.584.500.500.644.475]
        
        Homozygous Familial Hypercholesterolemia [C18.452.584.500.500.644.475.500]

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]
        
        Hyperlipoproteinemia Type II [C18.452.584.563.481]
        
        Homozygous Familial Hypercholesterolemia [C18.452.584.563.481.500]

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]
        
        Hyperlipoproteinemia Type II [C18.452.648.398.481]
        
        Homozygous Familial Hypercholesterolemia [C18.452.648.398.481.500]

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Homozygous Familial Hypercholesterolemia

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