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…
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Microphthalmia-coloboma-rhizomelic skeletal dysplasia is a very rare genetic syndrome that affects eye development, bone growth, and sometimes the brain and other organs. “Microphthalmia” means one or...
Colobomatous microphthalmia-rhizomelic dysplasia syndrome is a very rare genetic condition that starts when the baby is still in the womb. In this syndrome, the eyes do...
Hypogenitalism means that the genitals stay too small and “child-like” for the person’s age. In simple words, the sex organs do not grow and mature in...
Colobomatous microphthalmia–obesity–hypogenitalism–intellectual disability syndrome is a very rare genetic condition. In this syndrome, both eyes are small (microphthalmia), one eye usually has a gap or missing...
MACOM syndrome means “macrophthalmia, colobomatous, with microcornea.” It is a very rare genetic eye problem. In this condition, the clear front window of the eye (cornea)...
Colobomatous macrophthalmia-microcornea syndrome is a very rare eye condition that is present from birth and runs in families. In this condition, the clear front window of...
Sorsby syndrome is a very rare genetic disease that affects both the eyes and the fingers and toes from birth. The main problems are a special...
Coloboma of macula–brachydactyly type B syndrome is a very rare genetic condition that affects both the eyes and the hands/feet from birth and lasts for life....
Collecting duct carcinoma of the kidney is a very rare and very aggressive type of kidney cancer. It starts in the last part of the kidney...
Kidney collecting duct carcinoma is a rare, very aggressive type of kidney cancer. It starts in the tiny tubes at the end of the kidney’s filtering...
Collagen VI-related muscular dystrophy is a group of rare genetic muscle diseases where the body makes collagen type VI in an abnormal way. Collagen VI is...
Collagen VI-related dystrophy is a group of rare genetic diseases that damage the muscles and the supporting tissues around them. In this condition, the body has...