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, usually benign tumor in the frontal sinus lining.
is a rare cancer that starts in the frontal sinus lining.
is inflammation of the frontal sinus, causing forehead pain and pressure.
is a rare genetic condition affecting development of the face and skull.
is a rare genetic disorder affecting bone growth and facial features.
is a rare genetic disorder affecting bone growth and body shape.
is a rare genetic disorder affecting bone growth, joints, and hearing.
is a rare abnormal blood vessel connection affecting the forehead and nose.
is a rare birth condition affecting development of the face and head.
is a rare genetic condition affecting facial and skull development before birth.
is a rare genetic condition affecting development of the face and head.
is a rare genetic condition affecting facial development, scalp hair, and genitals.
is a rare genetic condition affecting facial development and the upper limbs.
is a rare genetic condition affecting facial and eye development before birth.
is a rare genetic condition affecting the nose, eyes, and forehead.
is a group of brain disorders affecting behavior, language, and thinking.
is a progressive disorder causing early personality, behavior, and language changes (aphasia).
is an inherited disorder linking frontotemporal dementia and amyotrophic lateral sclerosis (ALS).
is a rare genetic condition causing frontotemporal dementia and/or amyotrophic lateral sclerosis.
is an inherited disorder that can affect behavior, language, movement, and muscles.
is a progressive genetic disorder combining frontotemporal dementia and ALS features.
is an inherited disorder causing frontotemporal dementia, amyotrophic lateral sclerosis, or both.