Find disease guides, symptoms, medicines, lab tests, and patient-friendly medical resources.
56,145 results found
Start with the most relevant medically organized result, then continue through conditions, tests, medicines, cancer knowledge, and patient guides.
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.
Cerebro-oculo-facio-skeletal (COFS) syndrome is a very rare genetic disease that affects the brain, eyes, face and bones from before birth. It is present at birth and...
Hypertrichosis, hyperkeratosis, intellectual disability, and distinctive facial features is a rare genetic condition that doctors now group under Coffin–Siris syndrome 1 (CSS1) or ARID1B-related Coffin–Siris syndrome....
ARID1B-related BAFopathy is a rare genetic brain-development condition. It happens when there are changes (variants) in a gene called ARID1B. This gene helps make a protein...
Coffin-Siris syndrome 1 is a very rare genetic condition that affects how a child grows and develops, especially the brain, face, fingers, and toes. It usually...
Short stature-onychodysplasia is a very rare genetic condition where a person is very short in height and has poorly formed nails (onychodysplasia). It usually belongs to...
Fifth digit syndrome is another name for Coffin–Siris syndrome. It is a rare genetic condition. It mainly affects the little finger or little toe (the fifth...
Dwarfism-onychodysplasia is another name for a rare genetic condition called Coffin–Siris syndrome. It is a disorder that affects many parts of the body, especially growth, nails...
Coffin-Siris syndrome is a rare genetic condition that affects many parts of the body, especially the brain, face, fingers, toes, hair, and growth. Children usually have...
X-linked dominant Coffin-Lowry syndrome is a rare genetic condition that affects how the brain, bones, and other body systems grow and work. It is present from...
Coffin-Lowry syndrome is a rare genetic condition that affects many parts of the body, especially the brain, face, bones, heart, and muscles. It usually causes learning...
Coenzyme Q10 deficiency disease is a rare health problem where the body does not have enough coenzyme Q10 (also called CoQ10 or ubiquinone). CoQ10 is a...
Coenzyme Q10 deficiency means the body does not have enough coenzyme Q10 (also called CoQ10 or ubiquinone). CoQ10 is a fat-like substance that sits inside tiny...
