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 neurologic disorder causing progressive movement, thinking, and nerve problems.
is a lifelong condition linked to prenatal alcohol exposure and brain differences.
is a childhood cancer of immature nerve cells, often adrenal glands.
is an outdated term for stress-related heart and circulation symptoms.
is a rare condition with extra pigment cells in skin and brain.
is a group of genetic conditions affecting skin, brain, and causing seizures.
is a rare inherited disorder causing progressive brain damage and movement problems.
is a rare childhood brain disorder causing balance, movement, and eye-movement problems.
is a group of inherited disorders causing iron buildup in the brain.
is a rare inherited disorder causing movement problems and progressive brain degeneration.
is a rare inherited disorder causing iron buildup and progressive movement problems.
is a group of conditions that gradually damage brain and nerve cells.
is a brain disorder causing involuntary movements, thinking problems, and mood changes.
is a group of brain disorders causing dementia and worsening daily function.
is a rare inherited brain disorder caused by poor folate transport.
is a long-lasting skin condition causing itchy, inflamed, and irritated patches.
is a genetic disorder affecting development, balance, muscle tone, and heart rhythm.
is a rare genetic disorder causing developmental delay, ataxia, and feeding problems.
is a rare genetic disorder affecting development, seizures, vision, bones, and balance.
is a neurodevelopmental disorder causing brain differences, poor growth, and facial changes.
is a rare genetic condition causing cataracts, poor growth, and developmental differences.
is a rare genetic condition affecting balance, coordination, and brain development.
is a rare genetic condition affecting development, facial features, and the brain.
is a rare neurodevelopmental disorder causing abnormal eye movements and poor coordination.