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 nerve disorder affecting swallowing and throat movement.
is a rare nerve disorder affecting swallowing, taste, and throat sensation.
is a rare tumor affecting a nerve for swallowing and throat sensation.
is paralysis of a nerve affecting swallowing, taste, and throat sensation.
is a rare nerve disorder causing severe throat, tongue, or ear pain.
is a cancer that starts in the vocal cords area.
is a cancer of the vocal cords in the voice box.
is a growth on the vocal cords that may be cancer.
is a throat cancer affecting the vocal cords in the voice box.
is a rare, slow-growing throat cancer affecting the vocal cords.
is a rare pancreatic neuroendocrine tumor that makes too much glucagon.
is a rare inherited disorder causing low cortisol and related health problems.
is bone loss caused by long-term steroid medicine use.
is an inherited disorder causing excess aldosterone and early high blood pressure.
is a rare inherited disorder that impairs making glucose, causing low blood sugar.
is a condition where the body has trouble processing sugar normally.
is a group of conditions that affect how the body uses sugar.
is a rare genetic condition that limits glucose delivery to the brain.
is a rare inherited disorder causing severe diarrhea from glucose and galactose.
is an inherited disorder causing red blood cells to break down.
is a rare inherited disorder that lowers glutathione and can cause anemia.
is a rare inherited metabolic condition involving buildup of glutaric acid.
is a rare inherited disorder that prevents proper breakdown of certain proteins.
is a rare inherited disorder that affects antioxidant protection and body chemistry.