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 birth defect affecting the anus and rectum alone.
is a birth defect causing an abnormally narrow anal opening.
is a rare birth defect causing an abnormal passage near the anus.
is a birth defect affecting the anus and rectum with a fistula.
is a birth defect where the rectum and colon develop abnormally.
is a rare birth defect where the rectum is blocked or missing.
is a birth defect where the rectum is abnormally narrow.
is a birth defect where the rectum connects abnormally to the urethra.
is a birth defect where the rectum connects abnormally to the vagina.
is a birth defect where the rectum connects abnormally to the bladder.
is a birth defect where the rectum opens near the vagina.
is a birth defect where the anus and rectum form abnormally.
is a skull condition where some baby skull bones fuse too early.
is a skull condition where some skull bones fuse too early.
is early fusion of both coronal skull seams without other syndrome signs.
is a rare skull condition where several head bones fuse too early.
is a rare skull condition where back head sutures close too early.
is a rare birth defect affecting how the airways branch.
is a brain or spinal cord structural difference without other syndromic features.
is a brain development disorder causing structural differences without other syndromic features.
is a rare brain development disorder caused by abnormal nerve cell movement.
is a rare birth defect affecting the urinary, genital, and intestinal openings.