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 skin, eye, and other birth differences.
is a rare mosaic disorder with linear skin lesions and systemic issues.
is thyroid tissue at the tongue base that can affect breathing.
is a movement disorder causing involuntary tongue, face, and mouth movements.
is a rare stomach cancer that stiffens and thickens the stomach.
is a cancer of the lip, often linked to sun, tobacco.
is an early, noninvasive lip cancer confined to surface cells.
is a broad term for conditions affecting the lips.
is a rare inherited disorder affecting body fat distribution and metabolism.
is a group of conditions affecting fat processing and cholesterol levels.
is a rare lung inflammation caused by fats or oils entering lungs.
is a group of inherited disorders that cause harmful fat buildup.
is a rare, aggressive bladder cancer subtype with lipid-rich tumor cells.
is a rare breast cancer with cells containing abundant fat-like material.
is a rare benign tumor made of fat and gland-like tissue.
is a rare diabetes type caused by severe loss of body fat.
is a rare, noncancerous fatty tumor that usually affects young children.
is a rare group of disorders causing loss of body fat distribution.
is a rare disorder causing abnormal body fat loss and metabolic problems.
is a rare genetic disorder causing fat loss, deafness, and learning disability.
is a rare soft tissue tumor with nerve-related and fatty features.
is a rare inherited disorder affecting energy production and causing severe symptoms.
is a rare inherited mitochondrial disease causing energy failure and lactic acidosis.
is a kidney disease that causes heavy protein loss in urine.