is a breast cancer driven by extra HER2 protein growth signals.

is a rare inherited skin disorder causing mottled, fragile skin changes.

is an inherited condition causing extra tryptase and sometimes allergy-like symptoms.

is an inherited disorder where abnormal proteins build up and damage organs.

is an inherited disorder causing abnormal protein buildup that mainly damages kidneys.

is a rare genetic disorder causing recurrent swelling of skin, gut, airway.

is an inherited disorder causing recurrent episodes of severe swelling.

is a rare inherited disorder causing repeated swelling from abnormal C1 inhibitor.

is a rare inherited disorder causing repeated swelling from low C1 inhibitor.

causes recurring episodes of deep swelling, often without hives or itching.

is a rare inherited disorder causing recurrent swelling of skin and airways.

is a rare inherited disorder causing recurrent swelling despite normal C1 inhibitor.

causes recurrent swelling episodes despite normal C1 inhibitor and no F12/PLG variant.

is a rare genetic disorder causing calcium buildup in arteries and joints.

is an inherited disorder that affects balance, coordination, and sometimes speech.

is an inherited disorder causing harmful protein buildup in nerves and organs.

is a rare inherited disorder causing white patches in eyes and mouth.

raises the risk of inherited breast, ovarian, and some other cancers.

is an inherited higher risk of breast cancer, often from gene changes.

is an inherited syndrome raising breast, ovarian, and other cancer risks.

is an inherited skin disorder causing blistering and later flat, dark spots.

is an inherited disorder causing extreme thirst and large amounts of urine.

is an inherited disorder causing amyloid buildup and bleeding in the brain.

is an inherited eye disorder that causes progressive vision loss.