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You searched for “X” in All. RX Search found 56,119 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
Syndromic sensorineural deafness due to combined oxidative phosphorylation defect is a very rare genetic disease. In this condition, a baby is born with permanent inner-ear hearing...
Combined oxidative phosphorylation deficiency 34 (COXPD34) is a very rare inherited disease where the tiny “power stations” inside cells, called mitochondria, do not make enough energy....
Epistaxis is the medical word for a nosebleed. It means that blood is coming out from inside the nose, from small blood vessels in the lining...
Combined oxidative phosphorylation deficiency caused by mutation in TXN2 is a very rare genetic disease that damages the tiny power stations in our cells, called mitochondria....
Combined oxidative phosphorylation deficiency 29 (often shortened to COXPD29) is a very rare genetic disease that hurts how the body makes energy inside cells. It mainly...
Combined oxidative phosphorylation deficiency caused by mutation in SLC25A26 is a very rare inherited mitochondrial disease. In this disease, both copies of a gene called SLC25A26...
Combined oxidative phosphorylation deficiency (often shortened to COXPD) is a group of very rare, inherited mitochondrial diseases. In this condition, several of the energy-making “machines” (called...
Combined oxidative phosphorylation deficiency caused by mutation in MRPL3 is a very rare genetic disease. It is a type of mitochondrial disease. In this condition, the...
Combined oxidative phosphorylation defect type 9 (COXPD9) is a very rare inherited disease of the tiny “power stations” inside our cells, called mitochondria. In this disease,...
Combined oxidative phosphorylation deficiency caused by mutation in AARS2 is a very rare inherited disease that mainly damages the tiny “power stations” inside cells, called mitochondria....
Combined oxidative phosphorylation defect type 8 (often written as COXPD8) is a very rare, very serious genetic disease that affects the tiny “power plants” inside our...
Severe C12orf65-related combined oxidative phosphorylation defect is a very rare inherited disease of the mitochondria. Mitochondria are tiny “power stations” inside almost every cell, and they...
