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56,142 results found
You searched for “Y” in All. RX Search found 56,142 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
Chronic stress isn’t something that arrives very loudly. It builds very slowly — and tight shoulders, having poor sleep, feeling constantly fatigue, feeling irritable, or just...
Antenatal abnormality means a problem in the baby that starts before birth and is found during pregnancy. Doctors often use this term for a structural problem,...
Enlarged nasopharyngeal tonsil means the adenoid has become bigger than normal. The adenoid is a patch of lymph tissue high at the back of the nose,...
Adenoid hypertrophy means the adenoids are bigger than normal. The adenoids are soft lymph tissue at the back of the nose, high in the throat, and...
Congenital enterocyte heparan sulfate deficiency is a very rare, severe, genetic intestinal disease. In this condition, the small bowel lining cells, called enterocytes, do not show...
Congenital enterocyte heparan sulfate deficiency is a real but ultra-rare genetic intestinal disease. It causes the small-intestine lining cells, called enterocytes, to lack heparan sulfate on...
Sprengel deformity is a birth condition in which one shoulder blade, called the scapula, stays higher than normal because it does not move down to its...
Congenital dyserythropoietic anemia, type III, also called CDA type III, is a very rare inherited blood disease. In this disease, the bone marrow tries to make...
Congenital dyserythropoietic anemia, type I, usually called CDA type I, is a rare inherited blood disease. In this disease, the bone marrow tries to make red...
Congenital dyserythropoietic anemia due to KLF1 mutation is a very rare inherited red blood cell disease. In most reported cases, doctors describe it as congenital dyserythropoietic...
Congenital dyserythropoietic anemia due to KLF1 mutation is a very rare inherited red blood cell disease. In most reported cases, doctors describe it as congenital dyserythropoietic...
Congenital dyserythropoietic anemia type 4, often called CDA type IV, is a very rare inherited red blood cell disorder linked to KLF1 dysfunction. In this disease,...
