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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 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...
Deficiency of molybdenum cofactor (often shortened to MoCD) is a very rare inherited disease. In this disease, the body cannot make a tiny helper molecule called...
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 malonic and methylmalonic acidemia (CMAMMA) is a very rare genetic disease. It happens when the body cannot handle two natural chemicals called malonic acid and...
Immunodeficiency with granulomatosis is a health problem where the immune system is weak and does not work in a normal way, and at the same time...
Combined immunodeficiency due to RAG1/2 deficiency is a serious inherited disease where the immune system cannot build normal T cells and B cells, which are the...
Combined immunodeficiency with skin granulomas is a rare inherited immune system disease. In this condition, both main arms of the adaptive immune system (T cells and...
