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 blood clot in a neck artery reducing brain flow.
is a rare neck cancer from cells near the carotid artery.
is a narrowing of neck carotid arteries, raising stroke risk.
is an immune reaction to carp, causing hives, swelling, or anaphylaxis.
is median nerve compression at the wrist causing hand numbness, tingling, weakness.
is median nerve compression at the wrist causing numbness and tingling.
is median nerve compression at the wrist causing numbness and weakness.
is a rare genetic disorder with craniosynostosis, facial differences, limb anomalies.
is a rare bone disorder causing cartilage-bone growths in wrists and ankles.
is a rare infection causing fever, severe anemia, and wart-like skin lesions.
is a cancer beginning in cartilage within bones; may spread.
is a rare inherited skeletal condition causing short limbs, sparse hair, immunodeficiency.
is a rare inherited disorder affecting heart rhythm, skin, and hair.
is an allergic skin reaction causing itchy, red rash after carvone exposure.
is a stomach shape variant that may cause fullness or reflux.
is a rare, noncancerous lymph node overgrowth with inflammatory symptoms.
is prostate cancer that grows despite low testosterone from hormone therapy.
is a rare genetic condition affecting eyes, ears, heart, kidneys, and growth.
is a bacterial infection from cats causing swollen lymph nodes, usually mild.
is clouding of the eye's lens that blurs vision over time.
is an inherited eye disorder causing lens clouding, with multiple forms.
is inherited lens clouding causing variable, often early-onset cataracts and vision loss.
is an inherited eye condition causing various cataract types and vision loss.
is an inherited lens clouding condition causing variable-onset vision impairment.