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Disease Info Card
Multiple Carboxylase Deficiency
Information about Multiple Carboxylase Deficiency: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Multiple Carboxylase Deficiency
Most recent studies have shown that Multiple Carboxylase Deficiency shares some biological mechanisms with acidemia, acidosis, acidosis-lactic, ataxia, biotin-deficiency, biotinidase-deficiency, exanthema, fetal-diseases, holocarboxylase-synthetase-deficiency, hyperammonemia, inborn-errors-of-metabolism, macular-corneal-dystrophy-type-i, metabolic-acidosis, metabolic-diseases, methylmalonic-acidemia, phenylketonurias, propionic-acidemia, pyruvate-carboxylase-deficiency-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Multiple Carboxylase Deficiency, and have been seen in publications frequently: Biotin Transport, Cell Division, Cellular Homeostasis, Coagulation, Dna Repair, Excretion, Fatty Acid Oxidation, Fatty Acid Transport, Gluconeogenesis, Histone Modification, Hypersensitivity, Intestinal Absorption, Localization, Mitosis, Pathogenesis, Regulation Of Gene Expression, Response To Biotin, Rna Splicing, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Multiple Carboxylase Deficiency, such as ACACA, ACADM, AMPD1, AMY2A, BLOC1S6, BTD, CSF2, CYCS, ECHDC1, EPB42, HLCS, LAMC2, MCC, MLYCD, MXD1, OTC, PAH, PC, PRH1. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.