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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 caused by mutation in ELAC2 is a very rare genetic disease that mostly affects the heart and brain.[1] It belongs to a...
Combined oxidative phosphorylation defect type 17 (also called COXPD17) is a very rare genetic disease that affects the tiny “power stations” inside cells, called mitochondria. In...
MTFMT combined oxidative phosphorylation deficiency is a rare inherited disease of the tiny “power plants” inside our cells, called mitochondria. In this disease, a gene named...
Combined oxidative phosphorylation deficiency caused by mutation in MTFMT (also called combined oxidative phosphorylation defect type 15 or COXPD15) is a very rare genetic disease that...
Combined oxidative phosphorylation defect type 15 is a very rare inherited disease that affects how the “power stations” of the cell, called mitochondria, make energy. In...
FARS2 combined oxidative phosphorylation deficiency is a very rare mitochondrial disease. It happens when a gene called FARS2 does not work properly, so the tiny “power...
Combined oxidative phosphorylation deficiency caused by mutation in FARS2 is a very rare genetic disease that affects how the “power plants” of the cell, called mitochondria,...
Combined oxidative phosphorylation defect type 14 (often written as COXPD14) is a very rare, serious genetic disease that affects how the tiny “power stations” inside our...
PNPT1 combined oxidative phosphorylation deficiency type 13 (often shortened to COXPD13) is a very rare genetic disease that mainly affects how the body’s cells make energy...
Combined oxidative phosphorylation deficiency caused by mutation in PNPT1 (also called COXPD13) is a very rare inherited mitochondrial disease. It happens when both copies of the...
Combined oxidative phosphorylation defect type 13 (often shortened to COXPD13) is a very rare genetic disease that affects how the tiny “power plants” inside our cells,...
RMND1 combined oxidative phosphorylation deficiency type 11 is a very rare genetic mitochondrial disease. It happens when both copies of a gene called RMND1 do not...
