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56,145 results found
You searched for “Y” in All. RX Search found 56,145 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
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...
Neonatal severe cardiopulmonary failure due to mitochondrial methylation defect is a very rare genetic disease that affects newborn babies. In this disease, the baby’s heart and...
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...
Combined oxidative phosphorylation deficiency caused by mutation in C12orf65 is a very rare genetic disease of the mitochondria, the “power plants” inside our cells. [1] It...
C12orf65 combined oxidative phosphorylation deficiency is a very rare genetic disease that affects how the “power stations” of the cell (mitochondria) make energy. In this condition,...
Combined oxidative phosphorylation defect type 7 is a very rare, inherited disease that affects how the tiny “power stations” in our cells (mitochondria) make energy. [1]...
