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 genetic condition causing delayed speech and facial differences.
is a genetic condition caused by missing DNA on chromosome 5.
is a very rare blood disorder involving abnormal IgD antibodies.
is an inherited hemoglobin disorder with high fetal hemoglobin and anemia.
is a genetic disorder causing progressive hip–shoulder weakness and cardiomyopathy.
is a mental health condition causing fixed false beliefs despite evidence.
is a syndrome of worsening memory, thinking, behavior, and daily function.
is brain damage from repeated head injuries, affecting memory, mood, and thinking.
is a skin condition caused by Demodex mites, often affecting eyelids.
is a condition that damages the protective covering around nerves.
is an inherited nerve disorder causing muscle weakness, numbness, and balance problems.
is nerve damage that strips protective myelin, causing weakness and numbness.
is a rare genetic condition causing developmental delays and intellectual disability.
is a rare immune disorder with too few dendritic cells.
is a rare cancer that begins in the body's dendritic immune cells.
is a rare cancer arising from the body's dendritic immune cells.
is a rare cancer of immune cells called dendritic cells.
is a mosquito-borne viral illness that can cause fever and pain.
is a mosquito-borne viral infection that causes fever, aches, and rash.
is a severe form of dengue causing bleeding, plasma leakage, and shock.
is severe dengue with dangerously low blood pressure and shock.
is a rare kidney disease caused by abnormal immune protein deposits.
is a platelet disorder that can cause easy bruising and bleeding.
is a rare inherited kidney disorder causing protein loss and kidney stones.