Faster access than browser!
11 relations: Amino acid, Blood plasma, Congenital disorders of amino acid metabolism, Fanconi syndrome, Glomerulus (kidney), Hartnup disease, Liver disease, Nephron, Phenylketonuria, Transport protein, Urine.
Amino acid
Amino acids are organic compounds containing amine (-NH2) and carboxyl (-COOH) functional groups, along with a side chain (R group) specific to each amino acid.
New!!: Aminoaciduria and Amino acid · See more »
Blood plasma
Blood plasma is a yellowish coloured liquid component of blood that normally holds the blood cells in whole blood in suspension; this makes plasma the extracellular matrix of blood cells.
New!!: Aminoaciduria and Blood plasma · See more »
Congenital disorders of amino acid metabolism
Inborn errors of amino acid metabolism are metabolic disorders which impair the synthesis and degradation of amino acids.
New!!: Aminoaciduria and Congenital disorders of amino acid metabolism · See more »
Fanconi syndrome
Fanconi syndrome or Fanconi's syndrome is a syndrome of inadequate reabsorption in the proximal renal tubules of the kidney.
New!!: Aminoaciduria and Fanconi syndrome · See more »
Glomerulus (kidney)
The glomerulus, plural glomeruli, is a network of capillaries known as a tuft, located at the beginning of a nephron in the kidney.
New!!: Aminoaciduria and Glomerulus (kidney) · See more »
Hartnup disease
Hartnup disease (also known as "pellagra-like dermatosis" and "Hartnup disorder") is an autosomal recessive metabolic disorder affecting the absorption of nonpolar amino acids (particularly tryptophan that can be, in turn, converted into serotonin, melatonin, and niacin).
New!!: Aminoaciduria and Hartnup disease · See more »
Liver disease
Liver disease (also called hepatic disease) is a type of damage to or disease of the liver.
New!!: Aminoaciduria and Liver disease · See more »
Nephron
The nephron (from Greek νεφρός – nephros, meaning "kidney") is the microscopic structural and functional unit of the kidney.
New!!: Aminoaciduria and Nephron · See more »
Phenylketonuria
Phenylketonuria (PKU) is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine.
New!!: Aminoaciduria and Phenylketonuria · See more »
Transport protein
A transport protein (variously referred to as a transmembrane pump, transporter, escort protein, acid transport protein, cation transport protein, or anion transport protein) is a protein that serves the function of moving other materials within an organism.
New!!: Aminoaciduria and Transport protein · See more »
Urine
Urine is a liquid by-product of metabolism in humans and in many animals.
New!!: Aminoaciduria and Urine · See more »
