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56,119 results found
You searched for “X” in All. RX Search found 56,119 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
Combined oxidative phosphorylation deficiency caused by mutation in TRMT5 is a very rare genetic disease of the mitochondria. Mitochondria are tiny parts inside each cell that...
Combined oxidative phosphorylation defect type 26 (COXPD26) is a very rare inherited disease that affects how the “power stations” of the cell, called mitochondria, make energy....
Combined oxidative phosphorylation deficiency caused by mutation in MARS2 is a very rare inherited mitochondrial disease. In this condition, a mistake (variant) in both copies of...
Combined oxidative phosphorylation defect type 25 (COXPD25) is a very rare genetic mitochondrial disease. It affects how the “power stations” of the cell, called mitochondria, make...
Combined oxidative phosphorylation defect type 24 (short form: COXPD24) is a very rare genetic disease that affects the “power plants” of the cell, called mitochondria. In...
GTPBP3 combined oxidative phosphorylation deficiency is a very rare genetic disease that affects how the tiny “power stations” in our cells, called mitochondria, make energy. In...
Combined oxidative phosphorylation deficiency caused by mutation in GTPBP3 is a very rare inherited mitochondrial disease. In medical databases it is usually called combined oxidative phosphorylation...
Combined oxidative phosphorylation defect type 23 (COXPD23) is a very rare genetic mitochondrial disease. It happens when both copies of a gene called GTPBP3 do not...
Combined oxidative phosphorylation deficiency caused by mutation in TARS2 is a very rare genetic mitochondrial disease. In medical books it is usually called combined oxidative phosphorylation...
Combined oxidative phosphorylation defect type 21 (often written as COXPD21) is a very rare genetic disease that damages the tiny power plants inside our cells, called...
Combined oxidative phosphorylation deficiency caused by mutation in VARS2 is a very rare genetic disease. Doctors also call it Combined oxidative phosphorylation deficiency 20 (COXPD20). In...
Combined oxidative phosphorylation defect type 20 (often written as COXPD20) is a very rare genetic disease that affects how the mitochondria in body cells make energy....
