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 cancer of the anal canal causing bleeding, pain.
is a rare, fast-growing cancer combining lining and connective tissue types.
is a rare, aggressive cervical cancer containing both carcinoma and sarcoma.
is a rare, aggressive uterine cancer with carcinoma and sarcoma components.
is a cancer at the stomach's top, near the esophagus.
involves abnormal left-right organ arrangement and congenital heart defects.
is a sudden loss of heart function requiring immediate CPR and defibrillation.
is a rare congenital heart outpouching that may cause complications.
is a rare, usually benign heart tumor from nerve-support cells.
is an inflammatory heart condition causing arrhythmias and heart failure.
is a medical emergency where fluid around the heart compresses it.
usually involves the pericardium (heart lining), causing inflammation and fluid buildup.
is a rare genetic disorder affecting heart and urogenital development.
is a rare inherited connective tissue disorder with severe heart valve disease.
is a rare genetic disorder causing heart defects and craniofacial abnormalities.
is a rare genetic condition affecting heart, facial features, skin, and development.
is a rare genetic disorder affecting the heart, face, skin, and development.
is a rare genetic disorder affecting heart, facial features, skin, development.
is a rare genetic condition affecting development, the heart, skin, and face.
is a medical emergency when the heart can't pump enough blood.
is a disease of the heart muscle affecting pumping and rhythm.
is a rare genetic disorder affecting heart muscle, eyes, hips, and spine.
is a rare genetic disorder causing cardiomyopathy, hypotonia, and lactic acidosis.