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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.
Combined immunodeficiency due to CD3-gamma (CD3γ) deficiency is a very rare, inherited disease of the immune system. In this condition, a small protein called CD3-gamma, which...
Combined deficiency of sialidase and beta-galactosidase is a rare inherited disease where two important “clean-up” enzymes inside the cell do not work properly. Doctors usually call...
Familial multiple coagulation factor deficiency is a group of rare inherited bleeding disorders where a person has low levels of two or more blood-clotting proteins at...
Combined deficiency of factor V and factor VIII is a rare inherited bleeding problem in which the blood has low levels of both factor V (FV)...
Elbow valgus deformity means the forearm points too far away from the body when the elbow is straight. Doctors also call this cubitus valgus. A small...
Varus flexion deformity means that a joint is bent in two ways at the same time.“Varus” means the lower part of the leg (or bone) points...
Varus elbow deformity means that the elbow is bent inward, so the forearm points toward the middle of the body instead of slightly away from it...
Primary chronic pseudo-obstruction of the colon is a long-lasting disease where the large bowel (colon) behaves as if it is blocked, but no real physical blockage...
Chorioretinopathy syndrome is a general name for eye diseases that damage both the retina (the light-sensing layer) and the choroid (the blood-vessel layer under the retina)....
Macular atrophy-chorioretinopathy syndrome is a very rare eye disease present from birth. In this disease the back part of the eye (the retina) and the layer...
Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome is a very rare, inherited eye disease. In this condition, the nerve head at the back of the eye (optic disc)...
Microphthalmia, syndromic type 14 is a very rare genetic disease that affects the eyes, bones, and body growth. In this condition, one or both eyes are...
