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 parasitic infection spread by mosquitoes and caused by worms.
is a rare, severe localized scleroderma causing deep skin and tissue hardening.
is inflammation of the spinal disc space, usually caused by infection.
is a chronic autoimmune skin condition causing round, scaly, often scarring rashes.
affects the eyelid skin, causing chronic inflammation, rash, and possible scarring.
is a heart condition where tissue below the aortic valve blocks flow.
is a heart condition causing narrowing below the aortic valve.
is a rare skin condition causing small, firm, waxy bumps.
is a rare genetic disorder causing multiple pituitary hormone deficiencies from birth.
is a rare genetic condition causing thickened skin on palms and soles.
is an inherited skin disorder causing thickened skin on palms and soles.
is a skin condition causing tiny thickened spots on palms and soles.
is a middle ear injury that can cause hearing loss.
is a rare genetic condition causing hip dislocation and unusual physical features.
is a rare allergy to the medicine disodium cromoglycate.
is an inherited condition that disrupts amino acid absorption and transport.
is an inherited metabolic disorder affecting how the body processes amino acids.
is a rare inherited condition affecting how the body processes asparagine.
is a rare inherited disorder affecting amino acid breakdown.
is a rare inherited condition that disrupts bile acid production.
is a group of conditions affecting bilirubin processing and removal.
is a rare inherited disorder affecting brain chemicals, movement, and development.
is a rare inherited disorder that impairs breakdown of certain amino acids.