Combined Oxidative Phosphorylation Deficiency 33 (COXPD33)

Combined Oxidative Phosphorylation Deficiency 33, also known as coxpd33, is related to mitochondrial metabolism disease and coenzyme q10 deficiency disease. An important gene associated with Combined Oxidative Phosphorylation Deficiency 33 is C1QBP (Complement C1q Binding Protein), and among its related pathways/superpathways are Signal Transduction and Prolactin Signaling. Affiliated tissues include kidney and liver, and related phenotypes are decreased activity of mitochondrial complex i and cardiomyopathy