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 pregnancy-related autoimmune blistering skin condition causing intense itching.
is a rare autoimmune disease causing blisters and wart-like skin sores.
is an inherited condition causing early hearing loss and thyroid enlargement.
is a reaction to penicillin that may cause mild or severe symptoms.
is a fungal infection that mainly affects people with weakened immune systems.
is a rare birth difference where the penis does not develop.
is a noncancerous growth on the penis that usually stays localized.
is a broad term for conditions affecting the penis and its function.
is a rare cancer that starts in the tube carrying urine.
is a rare skin cancer affecting the penis, usually growing slowly.
is an uncommon, often aggressive type of penile squamous cell cancer.
is a rare cancer that starts in the tissues of the penis.
is an early penile cancer confined to the skin's top layer.
is a rare penile cancer with mixed squamous cell tumor features.
is a slow-growing, wart-like penile cancer that usually stays superficial.
is a rare skin cancer affecting the penis and nearby genital skin.
is a rare, usually slow-growing type of penile cancer.
is a rare penile cancer that usually starts in skin cells.
is a rare, slow-growing penile cancer that usually stays localized.
is a rare birth difference where the penis and scrotum develop abnormally.
is a rare genetic condition affecting development, brain function, and growth.
is a rare birth condition affecting the heart, breastbone, and abdomen.
is a rare chromosome condition causing developmental delays and medical problems.