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 genetic condition linked to cleft lip and palate.
is a genetic condition causing cleft lip, sometimes with cleft palate.
causes a cleft lip or palate with other facial differences.
is a rare facial birth difference affecting lip and mouth development.
is a rare genetic condition causing cleft lip, palate, and facial differences.
is a rare facial cleft affecting the mouth, lips, or nose.
is a rare birth difference causing facial clefts affecting the mouth.
is a genetic condition causing cleft lip, cleft palate, or both.
is a genetic condition causing cleft lip and/or cleft palate.
is a genetic condition causing cleft lip, cleft palate, and related features.
is a rare genetic disorder affecting the mouth, face, and fingers.
is a rare genetic disorder affecting the mouth, face, digits, and brain.
is a rare genetic disorder affecting face, mouth, and fingers/toes.
is a rare genetic disorder affecting facial, mouth, and finger development.
is a rare genetic disorder affecting the mouth, face, and digits.
is a rare genetic condition affecting facial, mouth, and finger development.
is a rare genetic condition affecting the mouth, face, and fingers.
is a rare genetic disorder affecting the face, mouth, fingers, and toes.
is a rare genetic syndrome causing oral-facial-limb differences and brain abnormalities.
is a rare genetic condition affecting facial, oral, and finger development.
is a rare genetic condition affecting mouth, face, digits, and brain.