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 broad term for problems affecting sexual function, health, or wellbeing.
is a condition involving sexual arousal linked to being humiliated or hurt.
involves intense sexual arousal from another person’s suffering or humiliation.
is a rare aggressive blood and skin cancer causing widespread rash.
is a rare aggressive blood and skin cancer affecting immune cells.
is pituitary gland damage after severe childbirth bleeding, causing hormone deficiencies.
is a rare genetic condition causing joint contractures and distinctive facial features.
is an immune reaction to shellfish that can be mild or severe.
is a serious illness causing anemia, kidney injury, and low platelets.
is a contagious intestinal infection that causes diarrhea, stomach cramps, and fever.
is a painful eye irritation caused by bright welding light exposure.
is a rare congenital heart condition causing multiple left-sided heart blockages.
is a digestive condition where too little small intestine causes poor absorption.
is a rare inherited disorder affecting how the body breaks down fat.
is a rare genetic condition causing short hand bones and insulin resistance.
is a rare inherited heart rhythm disorder that can cause dangerous arrhythmias.
is a rare genetic disorder affecting bone growth, limbs, and organs.
is a rare genetic disorder causing severe bone growth problems before birth.
is a rare, severe genetic disorder affecting bone growth before birth.
is a rare, severe genetic disorder affecting bone growth and organ development.
is a rare genetic disorder causing severe skeletal abnormalities before birth.
is a genetic disorder causing short ribs, extra fingers, and skeletal abnormalities.
is a rare genetic disorder reducing growth hormone (GH) release and height.
is a rare growth disorder caused by abnormal growth hormone action.