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 condition where maternal antibodies destroy a baby's red blood cells.
is a rare, severe inherited disorder affecting metabolism before birth.
is a pattern of birth defects and developmental problems from phenytoin exposure.
is a rare condition from too much iodine before birth.
is a blockage of the unborn baby's urinary tract before birth.
is a rare, usually noncancerous lung tumor seen before or after birth.
is a prenatal mercury poisoning disorder causing brain and nervous system damage.
is a rare birth defect pattern linked to minoxidil exposure during pregnancy.
is a term for possible health effects from nicotine exposure before birth.
is a rare fetal infection that can cause severe anemia and miscarriage.
is a rare birth defect pattern caused by trimethadione exposure during pregnancy.
is a group of birth differences caused by valproate exposure in pregnancy.
is sexual arousal linked to specific objects or body parts.
is a rare genetic disorder causing fever-triggered sudden liver failure in infants.
is a rare X-linked genetic condition causing developmental and neurological challenges.
is a rare genetic bone disorder causing curved limbs and growth problems.
is a group of genetic bone growth conditions affecting height and skeleton.
is a slow-growing brain tumor that starts in star-shaped support cells.
is a rare soft tissue cancer that starts in fat-forming cells.
is a rare condition causing joint pain, stiffness, and skin nodules.
is a rare, severe genetic disorder affecting bone and cartilage development.
is a rare inherited bone disorder causing very short limbs and chest.
is a rare genetic bone disorder causing severe short-limbed growth problems.
is a rare type of basal cell skin cancer.