Renal Aminoacidurias (Aminoaciduria, Renal)

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.
Also Known As:
Aminoaciduria, Renal; Renal Aminoaciduria; Aminoacidurias, Renal
Networked: 4 relevant articles (0 outcomes, 1 trials/studies)

Disease Context: Research Results

Related Diseases

1. Hypophosphatemia
2. Familial Hypophosphatemia (Phosphate Diabetes)
3. Glycosuria
4. Fanconi Syndrome (Syndrome, Fanconi)
5. Renal Tubular Acidosis (Distal Renal Tubular Acidosis)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Renal Aminoacidurias:
1. Uric Acid (Urate)IBA
2. Glucose (Dextrose)FDA LinkGeneric
3. D-Amino-Acid Oxidase (D-Amino Acid Dehydrogenase)IBA
4. Blood Proteins (Serum Proteins)IBA
5. Amino AcidsFDA Link