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 blockage of the small intestine after stomach surgery, causing pain.
is a rare inherited amyloidosis (protein deposits) causing progressive kidney failure.
is a liver cancer linked to aflatoxin toxin exposure from mold-contaminated foods.
is a fungal infection (mycosis) in Africa affecting skin, bones, lymph nodes.
is a tick-borne rickettsial infection causing fever, rash, and eschar.
is a tick-borne bacterial infection in sub-Saharan Africa causing fever, rash, eschar.
is a parasitic infection (sleeping sickness) spread by tsetse flies.
is a primary immunodeficiency with extremely low antibodies and recurrent infections.
is an inherited immune disorder causing absent antibodies (immunoglobulins) and recurrent infections.
is an inherited immune disorder causing absent antibodies (immunoglobulins) and infections.
is a rare inherited immune disorder with absent antibodies and recurrent infections.
is a rare inherited immune disorder causing very low antibodies and infections.
is a rare inherited immune disorder causing absent antibodies and recurrent infections.
is a rare inherited immune deficiency causing near-absent antibodies and recurrent infections.
is a rare inherited immunodeficiency with few B cells and infections.
is a rare genetic disorder with immune deficiency, microcephaly, craniosynostosis, dermatitis.
is a rare creatine deficiency disorder causing developmental delays and seizures.
is a progressive eye disease causing central vision loss in older adults.
is a retinal disease causing central vision loss in older adults.
is an inherited eye disorder affecting the macula, causing central vision loss.