rs2032582 is a genetic variant on gene ABCB1 associated with Inflammatory bowel disease 13.
rs10876864 is a genetic variant on gene IKZF4 associated with Intelligence and Allergic disease.
rs11540652 is a genetic variant on gene TP53 associated with Li-fraumeni syndrome 1 and Multiple myeloma.
rs104894226 is a genetic variant on gene HRAS associated with Costello syndrome and Large congenital melanocytic nevus.
rs7274581 is a genetic variant associated with Alzheimer's disease.
rs10808546 is a genetic variant associated with Abdominal aortic aneurysm.
is a rare cancer arising from the small intestine's inner lining.
is a rare stomach tumor that starts in the stomach lining.
is an uncommon growth in or around the eye, sometimes cancerous.
is a rare disorder causing missing or abnormal eyebrows and eyelashes.
is a rare eyelid positioning disorder affecting eyelid alignment and eye comfort.
is a rare inherited condition causing thickened heart muscle and heart problems.
describes uncommon conditions that make it harder for some women to conceive.
is a rare birth condition causing low hormone levels and infertility.
is a rare inherited adrenal disorder that can cause female infertility.
is a rare adrenal disorder that can cause infertility in females.
is a rare condition causing impaired ovarian function and difficulty conceiving.
is a rare genetic condition causing female infertility from abnormal ovarian function.
is a rare cause of female infertility where embryos cannot implant.
is a rare cause of female infertility due to underdeveloped ovaries.
is a rare cause of female infertility linked to hormone signaling problems.
is a rare genetic disorder affecting hormones needed for female fertility.
is a rare infertility condition where eggs do not mature properly.
is an uncommon Salmonella infection that can cause serious illness.
is a rare digestive system disorder affecting the stomach, intestines, or liver.
is an uncommon condition affecting the esophagus and stomach, causing digestive symptoms.
is a rare tumor where the esophagus meets the stomach.
is an inherited disorder affecting adrenal glands and hormone production.
is a rare genetic disorder affecting automatic body functions and nerves.
is a rare genetic disorder that affects bone growth and development.