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 pattern caused by thalidomide exposure during pregnancy.
is a severe genetic bone disorder that affects growth before birth.
is a severe genetic bone disorder causing short limbs and breathing problems.
is a severe genetic skeletal disorder usually fatal around birth.
is a rare ovarian cancer arising from hormone-producing theca cells.
is a tick-borne parasitic infection that can cause fever and anemia.
is an eye infection caused by parasitic worms.
is a blood cancer and bone marrow disorder linked to prior treatment.
is caused by too little vitamin B1 and can seriously affect nerves.
is a rare brain disorder that improves with vitamin B1 treatment.
is an inherited amino acid disorder that may improve with thiamine.
is a rare inherited disorder causing anemia, diabetes, and hearing loss.
is a rare inherited condition causing thickened earlobes and conductive hearing loss.
is a rare inherited corneal disorder causing recurrent erosions and blurry vision.
is a rare inherited disorder affecting finger and toe joint development.
is a rare genetic disorder affecting bone growth and facial features.
is a type of seizure that affects thoughts, awareness, or behavior.
is an allergic reaction to the anesthetic drug thiopental.
is an inherited condition affecting how the body processes thiopurine medicines.
is a rare birth difference affecting the neck and throat.
affects eye movement, eyelid lifting, and sometimes pupil size.
is a serious heart rhythm problem where signals fail to reach ventricles.
is a rare genetic condition causing developmental delay, microcephaly, and facial differences.
is a very rare genetic condition that can affect development.