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 genetic condition causing overgrowth, large head (macrocephaly), developmental delays, autism.
is a rare genetic disorder causing immune problems, albinism, and infections.
is a mouth cancer affecting inner cheek lining, causing sores and pain.
is lip inflammation causing dryness, cracking, pain from irritation, allergy, or infection.
is a rare inflammation of lip salivary glands causing swelling and crusting.
is a rare skeletal condition causing hand and spine enchondromas (benign tumors).
is an immune reaction to cherries causing itching, swelling, or anaphylaxis.
is a rare genetic jaw disorder with painless childhood swelling, often improving.
is a rare tumor of chest wall bones causing pain, swelling.
is a benign, slow-growing fatty lump under chest wall skin, usually harmless.
is a cancer of lymph cells affecting tissues of the chest wall.
is a rare soft-tissue tumor on the chest wall, usually slow-growing.
is optic chiasm damage causing side vision loss (bitemporal hemianopia), often tumor-related.
is an immune reaction to egg proteins, sometimes causing severe allergic reactions.
is a contagious viral illness causing itchy blisters, fever, and fatigue.
is a benign parathyroid tumor causing high blood calcium (hypercalcemia).
is a mosquito-borne viral illness causing sudden fever and severe joint pain.
is a skin lupus causing cold-triggered, painful finger and toe sores.
is a rare genetic disorder affecting the skin and limbs, often one-sided.
is a seizure disorder causing brief staring spells and unawareness in children.
is a fast-growing blood cancer of lymphocytes starting in bone marrow.
is a rare, aggressive childhood blood cancer affecting platelet-forming bone marrow cells.
is a fast-growing blood and bone marrow cancer in children.
is a rare, fast-growing cancer of blood or lymph vessels.