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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.
TUFM combined oxidative phosphorylation deficiency (also called combined oxidative phosphorylation deficiency type 4, COXPD4) is a very rare genetic disease of the mitochondria, the “power plants”...
Combined oxidative phosphorylation deficiency caused by mutation in TUFM is a very rare genetic disease that affects how the tiny “power stations” of the cell, called...
Combined oxidative phosphorylation defect type 4 is a very rare genetic disease of the mitochondria, the tiny “power plants” inside our cells. In this condition, the...
Combined oxidative phosphorylation deficiency caused by mutation in TRMT10C is a very rare inherited mitochondrial disease. In this disease, changes (mutations) in the TRMT10C gene damage...
Combined oxidative phosphorylation defect type 30 is an ultra-rare inherited disease of the mitochondria, which are the “power stations” inside each cell. In this disease, the...
Combined oxidative phosphorylation defect type 27 (COXPD27) is a very rare inherited disease where the “power stations” of the cell, called mitochondria, cannot make enough energy...
Combined oxidative phosphorylation deficiency caused by mutation in CARS2 (also called combined oxidative phosphorylation deficiency 27, COXPD27) is a very rare genetic disease that affects how...
Combined oxidative phosphorylation defect type 27 (often shortened to COXPD27) is a very rare genetic disease that damages the tiny power stations inside our cells, called...
Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay (often shortened to PNSED) is a very rare genetic disease that mainly affects the nerves, muscles,...
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...
