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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.
Retinal cone dystrophy type 3B is a very rare inherited eye disease that mainly damages the cone cells in the retina, which are the light-sensitive cells...
Cone dystrophy with supernormal scotopic electroretinogram is a rare, inherited eye disease that mainly damages the cone cells in the retina, and later also affects the...
Cone dystrophy with supernormal rod electroretinogram is a rare eye disease that damages the light-sensing cells in the retina, especially the cone cells in the center...
Cone dystrophy with supernormal rod response (CDSRR) is a very rare inherited eye disease where the cone cells in the retina slowly stop working properly, and...
Cone dystrophy is a rare eye disease where the cone cells in the retina slowly stop working properly. Cone cells are the light-sensing cells that help...
Jackson-Barr syndrome is a very rare genetic condition that affects hearing, the eyelids, the skeleton (bones and joints), and some parts of the skin, hair, and...
Conductive hearing loss-ptosis-skeletal anomalies syndrome is a very rare genetic condition. In this syndrome, the tiny passages and bones in the outer and middle ear do...
Conductive deafness–ptosis–skeletal anomalies syndrome is a very rare genetic syndrome where a person is born with a block in the sound-path of the ear (conductive hearing...
Mengel-Konigsmark syndrome is a very rare genetic disorder present from birth. It is mainly known for conductive hearing loss and abnormal outer ear shape. In many...
Conductive hearing loss-malformed external ear syndrome is a very rare genetic syndrome present from birth. It mainly affects the outer ear and the middle ear sound-conducting...
Conductive deafness–malformed external ear syndrome is a very rare genetic condition in which the outer ear (pinna and/or ear canal) does not form in the usual...
Compton-North congenital myopathy (also called congenital lethal myopathy, Compton-North type or MYPCN) is an extremely rare genetic muscle disease that starts before birth and is usually...
