Chronic Diarrhea – Causes, Symptoms, Diagnosis, Treatment
Chronic diarrhea is defined as the passage of loose or liquid stools, watery stools three or more times a day for at least 4…
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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.
Primary extrapulmonary coccidioidomycosis is an infection caused by a fungus called Coccidioides that shows itself first outside the lungs, such as in the skin, bones, joints,...
Coccidioidomycosis is a lung infection caused by a fungus called Coccidioides. This fungus lives in dry, dusty soil. When the soil is disturbed, tiny fungal spores...
Lissencephaly type 5 (often written as LIS5) is a very rare genetic brain problem where the surface of the brain does not form normal folds and...
Lissencephaly type 2 without muscular or eye involvement is a very rare brain development problem present from birth. Doctors also call it cobblestone lissencephaly without muscular...
Cobblestone lissencephaly without muscular or ocular involvement is a very rare brain development problem that starts before birth. In this condition, the surface of the brain...
Lissencephaly type 2 is a very rare brain problem that starts before birth. In this condition, the baby’s brain surface does not form normal folds and...
Cobblestone lissencephaly is a rare brain malformation where the surface of the brain looks bumpy and uneven, like small stones on a road. In this condition,...
Spinal arteriovenous metameric syndrome (SAMS) is a very rare birth-time (congenital) blood vessel problem that affects one body segment of the spine and the tissues linked...
Cobb syndrome is a very rare condition where a child or adult has abnormal blood vessels in the skin and in the spine in the same...
Cerebroretinal microangiopathy with calcifications and cysts is a very rare inherited disease that mainly damages the tiny blood vessels in the brain and the back of...
Cerebroretinal microangiopathy with calcifications and cysts (often shortened to CRMCC) is a very rare inherited disorder that mainly affects the brain and the eyes, and can...
Coats plus syndrome is a very rare, inherited, multi-system disease where tiny blood vessels (especially in the retina of the eye and the brain) are abnormal...