Medical dictionary. 2011.
p-hydroxyphenylacetate — A minor side product of l tyrosine degradation that is elevated in the urine in cases of neonatal tyrosinemia and in Richner Hanhart syndrome … Medical dictionary
Glycine encephalopathy — (Non ketotic Hyperglycinemia) Classification and external resources Glycine OMIM 605899 … Wikipedia
List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… … Wikipedia
Citrullinemia — Classification and external resources Citrulline ICD 10 E72.2 … Wikipedia
N-Acetylglutamate synthase deficiency — Classification and external resources N Acetylglutamic acid OMIM 237310 … Wikipedia
metabolic 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… … Universalium
Iminoglycinuria — Classification and external resources Imine, a functional group found in imino acids ICD 10 E72.0 … Wikipedia
Phenylketonuria — PKU redirects here. For other uses, see PKU (disambiguation). Phenylketonuria Classification and external resources ICD 10 E70.0 ICD 9 … Wikipedia
Methylmalonic acidemia — Classification and external resources Methylmalonic acid ICD 10 E … Wikipedia
Oculocutaneous albinism — Classification and external resources ICD 10 E70.3 ICD 9 270.2 … Wikipedia
