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 an immune reaction to proteins in goat milk.
is a rare, often aggressive appendix cancer with mixed tumor features.
is an enlarged thyroid causing neck swelling and possible hormone imbalances.
is a rare inherited condition causing developmental delays and severe constipation.
is a rare condition affecting facial development, often involving eyes and ears.
is a rare inherited retinal disorder causing night blindness and vision loss.
is a rare birth condition affecting the arms and legs.
is a rare condition affecting brain development, facial sensation, and scalp hair.
affects the ovaries or testes, disrupting hormones, fertility, or development.
is a condition where the ovaries or testes do not fully develop.
is a disorder where the ovaries do not develop typically.
is a rare tumor that starts in the ovaries or testicles.
is a rare tumor in abnormal gonads, often linked to Y chromosome.
is a joint-area bursa infection caused by gonorrhea bacteria.
is a serious eye infection caused by gonorrhea bacteria.
is a vision-threatening eye infection from Neisseria gonorrhoeae, needing urgent antibiotics.
is an eye inflammation caused by gonorrhea bacteria entering the eye.
is a rare eye infection caused by gonorrhea bacteria.
is a rare gonorrhea-related infection of the seminal vesicles.
is a rare spinal infection caused by gonorrhea bacteria.
is a joint infection from gonorrhea that causes pain and swelling.
is a common sexually transmitted infection that often causes no symptoms.
is a rare immune disorder linked to thymoma and frequent infections.
is a very rare genetic condition affecting development and physical features.