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 early-onset diabetes caused by NEUROD1 gene changes.
is an inherited early-onset diabetes caused by KLF11 gene changes.
is an inherited form of diabetes that often begins in adolescence.
is an inherited diabetes type caused by changes in PAX4.
is a rare abnormal tangle of blood vessels in the upper jaw.
is a cancer that starts in the upper jaw or nearby sinuses.
is a rare cancer of gland cells in the maxillary sinus.
is a rare cancer of the sinus that can grow slowly.
is a noncancerous growth in the cheekbone sinus.
is a rare cancer that starts in the cheek-area sinus.
is a rare growth of skin cells in the maxillary sinus.
is a rare noncancerous nasal tumor that can grow and recur.
is a rare benign tumor in the lining of the maxillary sinus.
is a rare cancer starting in the lining of the maxillary sinus.
is an infection or inflammation of the air-filled space behind your cheek.
is a rare birth condition affecting the nose and upper jaw.
is a condition where the vagina and uterus do not fully develop.
is a birth condition with missing uterus and upper vagina only.
is a rare condition affecting the uterus, vagina, and other organs.
is a rare disorder causing fibrous dysplasia and soft-tissue myxomas.
is a rare genetic disorder affecting bones, skin pigmentation, and hormones.
is a rare genetic disorder affecting bones, skin, and hormone-producing glands.
is an aggressive type of non-Hodgkin lymphoma, often linked to genetic changes.
is a rare genetic condition affecting growth, development, and physical features.