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 congenital condition where the anus and rectum form abnormally.
is a narrowing of the anus or rectum causing difficult bowel movements.
is an eating disorder causing restricted intake, weight loss, and health complications.
is lack of awareness of one’s illness, common in neurologic conditions.
is a birth defect with absent external ear (pinna), affecting hearing.
is when ovaries don't release an egg, causing irregular periods and infertility.
is a rare genetic condition causing elbow webbing and limited arm movement.
is a rare genetic muscle disorder causing prenatal contractures and respiratory weakness.
is a stroke affecting inner frontal brain, causing leg weakness, confusion.
is a painful lower-leg condition where pressure reduces blood flow, damaging tissues.
is pigment deposits on the cornea’s front surface, sometimes affecting vision.
is a usually benign tumor from meninges at the frontal skull base.
is a trapped nerve causing chronic, localized abdominal wall pain.
is the lens shifting forward into the eye’s front chamber, impairing vision.
is a usually benign tumor at skull base compressing brainstem/spinal cord.
affects spinal cord nerve cells, causing progressive muscle weakness, wasting, and cramps.
causes sudden, painless vision loss due to reduced optic nerve blood flow.
is a genetic disorder causing protruding upper jaw, crossed eyes, intellectual disability.
is a benign meningeal tumor compressing the anterior optic pathway, impairing vision.
is painful inflammation of the front eye white (sclera), risking vision.
is an eye development disorder affecting anterior segment with systemic features.
is an eye development disorder affecting cornea, iris, and drainage structures.
is a genetic eye disorder affecting front structures and vision.
is an eye development disorder affecting front structures, without problems elsewhere.