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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.
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...
Combined oxidative phosphorylation deficiency caused by mutation in RMND1 is a very rare inherited disease in which the tiny “power stations” of the cell (mitochondria) cannot...
Combined oxidative phosphorylation defect type 11 (often shortened to COXPD11) is a very rare, inherited disease that affects the “power stations” of the body’s cells, called...
Xanthine oxidase–sulfite oxidase deficiency is a very rare, serious genetic disease. In this condition, two important enzymes in the body, xanthine oxidase (also called xanthine dehydrogenase)...
Sulfite oxidase deficiency due to molybdenum cofactor deficiency is a very rare genetic disease. In this condition, the body cannot make a small helper molecule called...
Hereditary xanthinuria type 2 is a very rare, life-long (genetic) disease of purine metabolism, which is the way the body breaks down some building blocks of...
Combined xanthine oxidase and aldehyde oxidase deficiency is a very rare inherited problem with body chemistry. In this condition, two enzymes called xanthine oxidase (or xanthine...
Combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase is a very rare, serious inherited metabolic disease. In simple words, the body cannot make a...
Combined immunodeficiency with expansion of gamma delta T cells (often shortened to CID with γδ T-cell expansion) is a rare group of primary (inborn) immune system...
Combined immunodeficiency due to OX40 deficiency is a very rare inherited disease of the immune system. In this condition, a gene called TNFRSF4, also known as...
