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 noncancerous pituitary tumor that makes too much hormone.
is a noncancerous pituitary tumor that may cause hormone and vision problems.
is an inherited retinal disorder causing night blindness and delayed dark adaptation.
is an inherited eye condition that can gradually affect central vision.
is a rare inherited eye condition causing tiny retinal spots.
is a yeast or fungal infection of the swallowing tube (esophagus).
is a rare stomach infection caused by fungi.
is a fungal infection caused by different types of fungi.
is an eye infection of the cornea caused by fungi.
is a rare fungal infection causing inflammation around the brain and spine.
is a rare fungal infection that inflames and damages muscle tissue.
is inflammation of the umbilical cord, usually linked to infection.
is a skin infestation caused by fly larvae developing under the skin.
is a skin infestation by tumbu fly larvae causing boil-like sores.
is a skin infestation where fly larvae cause painful boil-like sores.
is a skin infestation where botfly larvae grow under the skin.
is a fungal infection that can affect skin, eyes, or blood.
is a dental difference where two lower front teeth are joined.
is a rare inherited disorder causing seizures, low muscle tone, developmental delays.
is a rare genetic condition affecting development, learning, behavior, and physical features.
is a condition with concentrated blood from low plasma volume.
causes trouble starting and controlling walking despite normal strength.
is an inherited disorder that impairs galactose processing and often causes cataracts.
is a rare inherited disorder that affects how the body processes galactose.