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 newborn condition causing high ammonia levels soon after birth.
is a temporary delay in making enough antibodies during infancy.
is a temporary delay in antibody production during early infancy.
is rare infant disorder causing high triglycerides and fatty liver, often improving.
causes temporary abnormal blood cell growth, usually in newborns with Down syndrome.
is a rare form of diabetes in newborns that usually goes away.
is a rare newborn metabolic disorder that temporarily affects energy production.
is a temporary muscle weakness in newborns caused by maternal antibodies.
is a temporary low neutrophil count in newborns that usually resolves.
is a temporary low platelet count in some newborn babies.
is a temporary condition causing salt loss and dehydration in infants.
is a temporary change in eyesight caused by shifts in focusing.
is a brief blockage of blood flow to the retina.
is a temporary newborn condition causing high tyrosine levels that usually resolves.
is a cancer that usually starts in the urinary tract lining.
is a rare type of uterine cancer arising from the womb lining.
is a rare fatty growth near the lower spinal cord.
is a rare, usually benign growth in the urinary tract lining.
is a rare inherited disorder affecting vitamin B1 use and energy production.
is a birth heart defect with switched main arteries, needing early surgery.
is a serious congenital heart defect with the two main arteries switched.
is a cancer in the middle part of the large intestine.
is a rare condition causing spinal cord inflammation and nerve symptoms.
is a rare birth difference where tissue blocks part of the vagina.