Biomaterial Database

Riboflavin responsive glutaric aciduria type II. 1990

N Gregersen, and W Rhead, and E Christensen

University Department of Clinical Chemistry, Aarhus Kommunehospital, Denmark.

UI	MeSH Term	Description	Entries
D008661	Metabolism, Inborn Errors	Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero.	Inborn Errors of Metabolism,Metabolism Errors, Inborn,Error, Inborn Metabolism,Errors Metabolism, Inborn,Errors Metabolisms, Inborn,Errors, Inborn Metabolism,Inborn Errors Metabolism,Inborn Errors Metabolisms,Inborn Metabolism Error,Inborn Metabolism Errors,Metabolism Error, Inborn,Metabolism Inborn Error,Metabolism Inborn Errors,Metabolisms, Inborn Errors
D005977	Glutarates	Derivatives of glutaric acid (the structural formula (COO-)2C3H6), including its salts and esters.	Glutarate
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D006943	Hyperglycemia	Abnormally high BLOOD GLUCOSE level.	Postprandial Hyperglycemia,Hyperglycemia, Postprandial,Hyperglycemias,Hyperglycemias, Postprandial,Postprandial Hyperglycemias
D000138	Acidosis	A pathologic condition of acid accumulation or depletion of base in the body. The two main types are RESPIRATORY ACIDOSIS and metabolic acidosis, due to metabolic acid build up.	Metabolic Acidosis,Acidoses,Acidoses, Metabolic,Acidosis, Metabolic,Metabolic Acidoses
D012256	Riboflavin	Nutritional factor found in milk, eggs, malted barley, liver, kidney, heart, and leafy vegetables. The richest natural source is yeast. It occurs in the free form only in the retina of the eye, in whey, and in urine; its principal forms in tissues and cells are as FLAVIN MONONUCLEOTIDE and FLAVIN-ADENINE DINUCLEOTIDE.	Vitamin B 2,Vitamin G,Vitamin B2
D012257	Riboflavin Deficiency	A dietary deficiency of riboflavin causing a syndrome chiefly marked by cheilitis, angular stomatitis, glossitis associated with a purplish red or magenta-colored tongue that may show fissures, corneal vascularization, dyssebacia, and anemia. (Dorland, 27th ed)	Deficiency, Riboflavin,Deficiencies, Riboflavin,Riboflavin Deficiencies
D042964	Acyl-CoA Dehydrogenase	A flavoprotein oxidoreductase that has specificity for medium-chain fatty acids. It forms a complex with ELECTRON TRANSFERRING FLAVOPROTEINS and conveys reducing equivalents to UBIQUINONE.	Acyl-coenzyme A Dehydrogenase,Fatty-acyl CoA Dehydrogenase,MCACA-Dehydrogenase,Medium Chain Acyl-CoA Dehydrogenase,Medium-Chain Acyl-CoA Dehydrogenase,Medium-Chain Acyl-Coenzyme A Dehydrogenase,Octanoyl-CoA Dehydrogenase,Palmitoyl-CoA Dehydrogenase,Acyl CoA Dehydrogenase,Acyl coenzyme A Dehydrogenase,Acyl-CoA Dehydrogenase, Medium-Chain,CoA Dehydrogenase, Fatty-acyl,Dehydrogenase, Acyl-CoA,Dehydrogenase, Acyl-coenzyme A,Dehydrogenase, Fatty-acyl CoA,Dehydrogenase, Medium-Chain Acyl-CoA,Dehydrogenase, Octanoyl-CoA,Dehydrogenase, Palmitoyl-CoA,Fatty acyl CoA Dehydrogenase,MCACA Dehydrogenase,Medium Chain Acyl CoA Dehydrogenase,Medium Chain Acyl Coenzyme A Dehydrogenase,Octanoyl CoA Dehydrogenase,Palmitoyl CoA Dehydrogenase
D044943	Fatty Acid Desaturases	A family of enzymes that catalyze the stereoselective, regioselective, or chemoselective syn-dehydrogenation reactions. They function by a mechanism that is linked directly to reduction of molecular OXYGEN.	Acyl CoA Desaturase,Enoyl CoA Reductase,Fatty Acid Desaturase,Fatty Acid Desaturating Enzymes,Acyl CoA Desaturases,Enoyl CoA Reductases,Acid Desaturase, Fatty,CoA Desaturase, Acyl,CoA Reductase, Enoyl,Desaturase, Acyl CoA,Desaturase, Fatty Acid,Desaturases, Fatty Acid,Reductase, Enoyl CoA,Reductases, Enoyl CoA