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.
involves wearing clothes traditionally associated with another gender expression.
is a rare inherited muscle disorder causing progressive hip and shoulder weakness.
is bone tissue death caused by lost blood flow after injury.
is brain damage caused by a sudden blow, jolt, or penetrating injury.
is eye damage after injury that raises pressure and threatens vision.
is a genetic condition that affects facial bone and tissue development.
is a genetic condition affecting facial development, often causing hearing loss.
is a rare genetic condition affecting development of the face and ears.
is a genetic craniofacial condition causing facial bone underdevelopment and hearing loss.
is a rare genetic condition affecting facial bone and tissue development.
is a genetic condition affecting facial bone development before birth.
is a rare inherited condition that makes digesting trehalose sugar difficult.
is a rare genetic disorder causing tremor, ataxia, and low brain myelin.
is a rare inherited condition causing tremor, eye movements, and duodenal ulcers.
is a bacterial infection spread by body lice, often causing recurring fever.
is a rare heart defect with an extra membrane dividing an atrium.
is a rare inherited disorder that disrupts how cells make energy.
is a parasitic infection from undercooked meat causing fever and muscle pain.
is a parasitic infection from eating undercooked pork or wild game.
is a rare genetic condition affecting hair, teeth, and bones.
is a rare genetic disorder affecting hair, eyes, teeth, and fingers.
is a rare genetic condition mainly affecting hair, teeth, and nails.
is a rare genetic condition affecting hair, skin, and tooth development.
is a rare genetic syndrome affecting hair, teeth, and development.