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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.
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,...
Congenital dyserythropoietic anemia, or CDA, is a rare inherited blood disease. In this disease, the bone marrow makes red blood cells in an abnormal way. Many...
HEMPAS – Hereditary Erythroblast Multinuclearity with Positive Acid Serum Test is a rare inherited blood disease. Its full old name is hereditary erythroblastic multinuclearity with positive...
Congenital dyserythropoietic anemia type 2, also called CDA type II, is a rare inherited blood disease. In this disease, the body makes red blood cells in...
Congenital dyshaematopoietic anemia is more commonly called congenital dyserythropoietic anemia, or CDA. It is a rare inherited blood disorder. In this disease, the bone marrow makes...
Congenital dyserythropoietic anemia, often called CDA, is a rare inherited blood disorder. In this disease, the bone marrow makes red blood cells in an abnormal way....
Component of oligomeric Golgi complex 2–congenital disorder of glycosylation is usually called COG2-CDG. It is a very rare inherited metabolic disease. In this disease, both copies...
Congenital disorder of glycosylation, type IIq, is a very rare inherited metabolic disease. It is now also commonly called COG2-CDG because it is caused by harmful...
DPM1-CDG means dolichyl-phosphate mannosyltransferase 1 catalytic subunit congenital disorder of glycosylation. It is a very rare inherited metabolic disease. In this condition, the DPM1 gene does...
Dolichol-phosphate-mannose synthase 1 deficiency is a very rare inherited disease. Doctors also call it DPM1-CDG. It belongs to a group called congenital disorders of glycosylation, or...
