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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 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....
Combined oxidative phosphorylation deficiency caused by mutation in MRPS16 is a very rare, serious genetic disease of the mitochondria, the “power plants” inside our cells.[1] In...
Combined oxidative phosphorylation defect type 2 (often written as combined oxidative phosphorylation deficiency 2 or COXPD2) is a very rare, very severe genetic disease of the...
Combined oxidative phosphorylation deficiency type 17 (often written as COXPD17) is a very rare genetic disease that affects the “power stations” of the cell, called mitochondria....
