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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.
Collagen 6-related myopathy (often written as collagen VI-related myopathy) is a rare inherited muscle disease. It happens when there is a change (mutation) in the genes...
Bone fragility-craniosynostosis-proptosis-hydrocephalus syndrome is an extremely rare genetic disease that mainly affects bones of the skull and the whole skeleton. Children have very weak bones that...
Cole-Carpenter syndrome is an extremely rare genetic bone disease. It affects less than a few dozen people in the world. In this condition, the bones are...
CRLF1-related cold-induced sweating syndrome, including Crisponi syndrome, is a very rare genetic disease that affects how the body controls temperature, sweating, face and limb shape, and...
Cold-induced sweating syndrome 1 (CISS1) is a very rare genetic disease that affects how the body controls temperature and how the nerves and face develop. In...
Sohar-Crisponi syndrome is a very rare genetic disease that mainly affects babies and children. It belongs to a family of problems called cold-induced sweating syndromes, which...
Crisponi syndrome is a very rare genetic disease. It starts in newborn babies. The baby has sudden strong muscle contractions, mainly in the face, neck, and...
Ciliary neurotrophic factor receptor-related disorder is another name for a very rare genetic disease called cold-induced sweating syndrome (CISS). It mainly affects how the autonomic nervous...
Cold-induced sweating syndrome (CISS) is a very rare genetic disease. It mainly affects how the body controls temperature, sweating, face muscles, and bones. Children with this...
Cohen-Gibson syndrome is a very rare genetic condition. It starts before birth or in early childhood. Children with this syndrome usually grow faster and bigger than...
Cutis verticis gyrata is a rare skin condition of the scalp where the skin becomes thick and forms deep folds and grooves that look like the...
Cohen syndrome is a very rare genetic condition that affects many parts of the body, especially growth, learning, eyes, blood cells, and body shape. It usually...
