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 fragile, abnormal gastrointestinal blood vessels causing recurrent bleeding and anemia.
is abnormal intestinal blood vessels causing painless bleeding and iron-deficiency anemia.
is sudden swelling under the skin from allergies, medications, or genetics.
are crack-like breaks in retinal layer that may affect vision.
are crack-like breaks in a deep retinal layer, risking vision loss.
is a rare T-cell lymphoma causing swollen lymph nodes and systemic symptoms.
is a benign skin growth from dilated blood vessels that may bleed.
is a rare, benign skin vascular lesion, often present from birth.
is a benign skin condition causing small, dark, bleeding-prone genital bumps.
is a benign skin condition with small, dark, wart-like vascular bumps.
is a benign fatty tumor with blood vessels, often tender lumps.
is a rare, benign skin vascular disorder causing tiny, snake-like red spots.
is a rare soft-tissue tumor of intermediate malignancy, typically affecting youth.
is a benign kidney tumor of blood vessels, muscle, and fat.
is a rare, benign vascular smooth muscle tumor causing tender skin lumps.
is a congenital vascular malformation disorder causing limb overgrowth and varicose veins.
is a rare congenital condition with abnormal blood vessels and bone undergrowth.
is a rare, aggressive cancer of blood or lymph vessel linings.
is a parasitic infection causing eosinophilic meningitis from rat lungworm.
is a sudden drainage blockage raising eye pressure, a vision-threatening emergency.
is a benign, localized patch of long, silky hair present at birth.
is inflammation at eye corners affecting eyelids and inner eye lining.
is painful inflammation at mouth corners causing cracks, redness, and irritation.
is a rare inherited condition with skin, immune, bone, and lymphatic problems.