Crigler-Najjar Syndrome

MeSH 搜索器

Crigler-Najjar Syndrome

A familial form of congenital hyperbilirubinemia transmitted as an autosomal recessive trait. It is characterized by icterus and brain damage caused by a glucuronyl transferase deficiency in the liver and faulty bilirubin conjugation.

推出的年份: 1991(1975)

树号: C16.320.565.300.281, C18.452.648.300.281

MeSH 单一 ID: D003414

进入的组:

Crigler Najjar Syndrome, Type 1
Crigler-Najar Syndrome
Crigler Najar Syndrome
Familial Nonhemolytic Unconjugated Hyperbilirubinemia
Hereditary Unconjugated Hyperbilirubinemia
Crigler Najjar Syndrome
Crigler-Najjar Syndrome, Type I
Crigler Najjar Syndrome, Type I

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Genetic Diseases, Inborn [C16.320]
      - Metabolism, Inborn Errors [C16.320.565]
        
        Hyperbilirubinemia, Hereditary [C16.320.565.300]
        
        Crigler-Najjar Syndrome [C16.320.565.300.281]
        
        Gilbert Disease [C16.320.565.300.528]
        
        Jaundice, Chronic Idiopathic [C16.320.565.300.764]

All MeSH Categories
- Diseases Category
  - Nutritional and Metabolic Diseases [C18]
    - Metabolic Diseases [C18.452]
      - Metabolism, Inborn Errors [C18.452.648]
        
        Hyperbilirubinemia, Hereditary [C18.452.648.300]
        
        Crigler-Najjar Syndrome [C18.452.648.300.281]
        
        Gilbert Disease [C18.452.648.300.528]
        
        Jaundice, Chronic Idiopathic [C18.452.648.300.764]

Like

分享书签

0 0 0 0 0 0 0

MeSH 搜索器

Crigler-Najjar Syndrome

副标题

留言 (0)