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 disorder with symmetric ring-like skin creases, sometimes delays.
is syphilis passed from a pregnant person to their baby before birth.
is an inborn abnormal connection between arteries and veins bodywide, disrupting circulation.
is a birth defect affecting major veins returning blood to the heart.
is jaw joint fusion (ankylosis) at birth, limiting mouth opening.
is a rare inherited blood disorder causing clots, low platelets, organ injury.
is a congenital thyroid structural difference with normal hormone levels (euthyroid).
is a rare heart defect where lung veins drain incorrectly, lowering oxygen.
is a parasitic infection acquired before birth, affecting brain and eyes.
is a rare birth defect narrowing the windpipe, causing breathing difficulty.
is a birth condition where weak windpipe cartilage collapses during breathing.
is a birth defect of the tricuspid heart valve affecting flow.
is a rare birth defect narrowing the tricuspid valve, obstructing right-heart flow.
is a birth defect of the heart’s tricuspid valve causing leakage.
is a rare birth condition causing facial numbness and corneal anesthesia.
is a birth-present eye-movement disorder causing vertical double vision and head tilt.
is a rare inherited intestinal disorder causing severe, lifelong infant diarrhea.
is a rare congenital heart defect causing severe mitral valve leakage.
causes one-sided lower lip weakness at birth (asymmetric crying facies).
is a birth defect where the urachus persists, causing umbilical drainage, infections.
is due to chickenpox in pregnancy, causing limb, eye, brain problems.
is a rare birth condition affecting blood vessels and bones.
is a birth condition with poor palate closure, causing hypernasal speech.
is a rare genetic disorder causing spine, heart, and kidney malformations.