Renal Aminoacidurias

MeSH 搜索器

Renal Aminoacidurias

A group of inherited kidney disorders characterized by the abnormally elevated levels of AMINO ACIDS in URINE. Genetic mutations of transport proteins result in the defective reabsorption of free amino acids at the PROXIMAL RENAL TUBULES. Renal aminoaciduria are classified by the specific amino acid or acids involved.

推出的年份: 2007(1963)

树号: C12.050.351.968.419.815.885, C12.200.777.419.815.885, C12.950.419.815.885, C16.320.831.885

MeSH 单一 ID: D000608

进入的组:

Aminoacidurias, Renal
Renal Aminoaciduria
Aminoaciduria, Renal

All MeSH Categories
- Diseases Category
  - Urogenital Diseases [C12]
    - Female Urogenital Diseases and Pregnancy Complications [C12.050]
      - Female Urogenital Diseases [C12.050.351]
        
        Urologic Diseases [C12.050.351.968]
        
        Kidney Diseases [C12.050.351.968.419]
        
        Renal Tubular Transport, Inborn Errors [C12.050.351.968.419.815]
        
        Acidosis, Renal Tubular [C12.050.351.968.419.815.093]
        
        Bartter Syndrome [C12.050.351.968.419.815.279]
        
        Dent Disease [C12.050.351.968.419.815.364]
        
        Fanconi Syndrome [C12.050.351.968.419.815.450]
        
        Gitelman Syndrome [C12.050.351.968.419.815.491]
        
        Glycosuria, Renal [C12.050.351.968.419.815.532]
        
        Hypophosphatemia, Familial [C12.050.351.968.419.815.647] add_circle
        
        Liddle Syndrome [C12.050.351.968.419.815.683]
        
        Oculocerebrorenal Syndrome [C12.050.351.968.419.815.720]
        
        Pseudohypoaldosteronism [C12.050.351.968.419.815.770]
        
        Renal Aminoacidurias [C12.050.351.968.419.815.885]
        
        Cystinuria [C12.050.351.968.419.815.885.250]
        
        Hartnup Disease [C12.050.351.968.419.815.885.625]

All MeSH Categories
- Diseases Category
  - Urogenital Diseases [C12]
    - Male Urogenital Diseases [C12.200]
      - Urologic Diseases [C12.200.777]
        
        Kidney Diseases [C12.200.777.419]
        
        Renal Tubular Transport, Inborn Errors [C12.200.777.419.815]
        
        Acidosis, Renal Tubular [C12.200.777.419.815.093]
        
        Bartter Syndrome [C12.200.777.419.815.279]
        
        Dent Disease [C12.200.777.419.815.364]
        
        Fanconi Syndrome [C12.200.777.419.815.450]
        
        Gitelman Syndrome [C12.200.777.419.815.491]
        
        Glycosuria, Renal [C12.200.777.419.815.532]
        
        Hypophosphatemia, Familial [C12.200.777.419.815.647] add_circle
        
        Liddle Syndrome [C12.200.777.419.815.683]
        
        Oculocerebrorenal Syndrome [C12.200.777.419.815.720]
        
        Pseudohypoaldosteronism [C12.200.777.419.815.770]
        
        Renal Aminoacidurias [C12.200.777.419.815.885]
        
        Cystinuria [C12.200.777.419.815.885.250]
        
        Hartnup Disease [C12.200.777.419.815.885.457]

All MeSH Categories
- Diseases Category
  - Urogenital Diseases [C12]
    - Urologic Diseases [C12.950]
      - Kidney Diseases [C12.950.419]
        
        Renal Tubular Transport, Inborn Errors [C12.950.419.815]
        
        Acidosis, Renal Tubular [C12.950.419.815.093]
        
        Bartter Syndrome [C12.950.419.815.279]
        
        Dent Disease [C12.950.419.815.364]
        
        Fanconi Syndrome [C12.950.419.815.450]
        
        Gitelman Syndrome [C12.950.419.815.491]
        
        Glycosuria, Renal [C12.950.419.815.532]
        
        Hypophosphatemia, Familial [C12.950.419.815.647] add_circle
        
        Liddle Syndrome [C12.950.419.815.683]
        
        Oculocerebrorenal Syndrome [C12.950.419.815.720]
        
        Pseudohypoaldosteronism [C12.950.419.815.770]
        
        Renal Aminoacidurias [C12.950.419.815.885]
        
        Cystinuria [C12.950.419.815.885.250]
        
        Hartnup Disease [C12.950.419.815.885.625]

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Genetic Diseases, Inborn [C16.320]
      - Renal Tubular Transport, Inborn Errors [C16.320.831]

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Renal Aminoacidurias

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