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 inherited eye condition causing early lens clouding (cataracts).
is an inherited eye disorder with variable lens clouding and vision loss.
is an inherited eye condition causing cataracts that can vary in type.
is a rare inherited eye condition causing early lens clouding.
is a rare genetic lens clouding causing blurred vision, often childhood.
is a clouding of the eye's lens causing blurry vision.
is a rare inherited lens clouding that impairs vision from childhood.
is a genetic eye condition causing lens clouding and blurry vision.
is a genetic eye condition causing childhood lens clouding and vision problems.
is a clouding of the eye’s lens causing blurred vision.
is a genetic eye condition causing lens clouding and vision loss.
is a genetic lens clouding, often inherited, causing cataracts and vision problems.
is a rare inherited cataract causing clouded lenses and vision problems.
is an inherited eye disorder causing lens clouding and vision problems.
is a genetic cataract with multiple patterns, impairing vision from lens clouding.
is an inherited eye condition causing clouding of the lens.
is a rare genetic disorder causing cataracts, oral frenula anomalies, growth delay.
is a genetic condition with cataracts, balance problems (ataxia), and hearing loss.
is a genetic syndrome causing cataracts, heart defects, and neural tube defects.
is a rare genetic disorder with cataracts, hearing loss, hypogonadism.
is a rare genetic eye disorder causing early cataracts and glaucoma.
is a rare genetic disorder affecting eyes, growth, nerves, hearing, and bones.
is a rare genetic disorder causing cataracts, excess hair (hypertrichosis), intellectual disability.
causes congenital cataracts, developmental delays, anal atresia, and urinary tract anomalies.