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 inherited ciliopathy affecting skull, hair, teeth, nails, kidneys.
is a rare genetic disorder affecting bone growth, hair, teeth, and kidneys.
is a rare genetic disorder affecting cilia, with skull, hair, kidney issues.
is a rare condition causing unusual facial features and cloudy eye lenses.
is a rare genetic condition affecting facial bone growth and tooth development.
is a rare genetic condition affecting facial features, bones, and learning.
is a rare genetic condition affecting facial development, growth, skin, and learning.
is a rare genetic disorder with facial differences, hearing loss, hand anomalies.
is a rare genetic condition affecting the face, skull, fingers, and toes.
is a genetic condition affecting skull, face, and limb development.
is a rare genetic condition affecting skull, facial, limb, and chest development.
is a rare inherited disorder affecting skull development and eye lenses.
is a rare genetic bone disorder affecting skull and long bones.
is a rare genetic bone disorder causing skull and facial overgrowth.
is a rare genetic disorder causing severe growth, skull, and limb abnormalities.
is a benign brain tumor near the pituitary, affecting hormones and vision.
is a severe neural tube defect affecting the brain and spine.
is a rare genetic condition affecting skull and nose development.
is a rare skull-growth disorder often linked with crossed eyes (strabismus).
is a birth condition where skull bones join too early.
is a genetic condition where skull joints (sutures) fuse too early.
is a rare condition causing early skull fusion, anal anomalies, and porokeratosis.
is a rare genetic condition causing skull, brain, and fluid buildup problems.