cystinuria
21Transport disease, cystine — Commonly known as cystinuria, this is an inherited (genetic) disorder of the transport of an amino acid (a building block of protein) called cystine. The result is an excess of cystine in the urine (cystinuria) and the formation of cystine stones …
22Cistinuria — Estructura química de la cistina formada por L cisteína (en condiciones biológicas) Clasificación y recursos externos …
23Tiopronin — drugbox IUPAC name = [(2 mercaptopropanoyl)amino] acetic acid CAS number = 1953 2 2 ATC prefix = R05 ATC suffix = CB12 PubChem = 5483 DrugBank = C = 5 | H = 9 | N = 1 | O = 3 | S = 1 molecular weight = 163.196 g/mol bioavailability = protein… …
24Lysinuric protein intolerance — Classification and external resources Lysine ICD 10 E …
25metabolic disease — ▪ pathology Introduction any of the diseases or disorders that disrupt normal metabolism, the process of converting food to energy on a cellular (cell) level. Thousands of enzymes participating in numerous interdependent metabolic pathways… …
26Cystine — An amino acid, one of the 20 amino acids which serve as the building blocks of protein. Cystine is not an essential amino acid, that is, it is not essential to the diet since the body can synthesize (make) it. Cystine is particularly notable… …
27penicillamine — A degradation product of penicillin; a chelating agent used in the treatment of lead poisoning, hepatolenticular degeneration, and cystinuria, and in the removal of excess copper in Wilson …
28Iminoglycinuria — Classification and external resources Imine, a functional group found in imino acids ICD 10 E72.0 …
29Genetic disorder — For a non technical introduction to the topic, see Introduction to genetics. Genetic disorder Classification and external resources MeSH D030342 A genetic disorder is an illness caused by abnormalities in genes or …
30Kidney stone — Classification and external resources …
