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Chronic diarrhea is defined as the passage of loose or liquid stools, watery stools three or more times a day for at least 4…
You searched for “Y” in All. RX Search found 56,145 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
Cognitive impairment – coarse facies – heart defects – obesity – pulmonary involvement – short stature – skeletal dysplasia syndrome is a very rare genetic disease....
Iris nevus syndrome is a rare eye disease where the front layer of the eye (the clear cornea and the colored iris) is changed by a...
Cogan-Reese syndrome is a very rare eye disease. It affects the clear front window of the eye (the cornea), the colored part (the iris), and the...
Oculovestibuloauditory syndrome is another name doctors sometimes use for Cogan’s syndrome. It is a rare autoimmune disease. “Autoimmune” means the body’s own defense system (immune system)...
Cogan syndrome is a rare disease where the body’s own defense system (the immune system) wrongly attacks parts of the eyes and inner ears. This attack...
Component of oligomeric Golgi complex 8 congenital disorder of glycosylation (often shortened to COG8-CDG) is a very rare inherited disease that affects how the body adds...
Carbohydrate deficient glycoprotein syndrome type IIh is a very rare inherited metabolic disease. It belongs to a group of diseases called congenital disorders of glycosylation (CDG)....
COG8-congenital disorder of glycosylation (COG8-CDG) is a very rare genetic disease. It happens when the COG8 gene does not work in the normal way. This gene...
Component of oligomeric Golgi complex 7 congenital disorder of glycosylation (COG7-CDG) is a very rare genetic disease that affects how the body adds sugar chains to...
Carbohydrate deficient glycoprotein syndrome type IIe is an extremely rare inherited disease of sugar processing inside the body’s cells. In today’s names it is usually called...
COG7-congenital disorder of glycosylation (COG7-CDG) is a very rare inherited disease that starts before birth and affects almost every part of the body. In this condition,...
Component of oligomeric Golgi complex 6–congenital disorder of glycosylation (short name COG6-CDG) is a very rare genetic disease that affects how sugar chains are added to...
