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 excess belly fat with metabolic changes raising diabetes and heart risks.
is an inherited disorder causing belly-centered obesity and early metabolic syndrome.
is a rare genetic disorder with abdominal obesity and metabolic syndrome features.
is a rare inherited disorder causing abdominal obesity and metabolic problems.
is tuberculosis (TB) infection of the abdomen causing pain, fever, weight loss.
is a tumor of the sixth cranial nerve (abducens), causing double vision.
is a nerve disorder causing outward eye weakness and double vision (diplopia).
is a rare inherited condition causing brain amyloid-beta (Aβ) buildup and dementia.
is a rare inherited disorder causing amyloid in brain vessels, strokes, dementia.
is a rare inherited brain vessel disease causing strokes and dementia.
is a rare inherited condition causing amyloid-beta buildup in brain blood vessels.
is amyloid protein buildup causing joint and tendon problems, often during dialysis.
is a rare genetic disorder with amyloid-beta deposits, often affecting brain.
is a rare disorder where amyloid protein builds up, harming organs.
is a rare inherited disorder causing fat malabsorption, nerve and eye problems.
is a rare genetic condition affecting facial, eyelid, skin, and genital development.
is a heart artery opening number abnormality, often present from birth.
is a rare congenital heart defect causing lung overcirculation and heart strain.
is a rare birth heart defect where a pulmonary artery misconnects.
is a problem with pupil reactions (pupillary reflex) to light and focus.
is the brain’s adaptation in strabismus (eye misalignment), reducing double vision.
involves reduced rod sensitivity, causing night blindness (nyctalopia) and poor dark adaptation.
is a hormone disorder causing irregular glucagon release and blood sugar imbalance.
is a rare inherited amyloid disorder of brain and blood vessels.