is a chronic inflammatory skin disorder causing thin, flat, discolored patches.

is a group of disorders causing progressive muscle wasting and weakness.

is a thinned, weakened eardrum after inflammation, sometimes reducing hearing.

is chronic nasal lining thinning with dryness, crusting, nosebleeds, unpleasant odor.

is thinning and dryness of vulvar tissue from low estrogen levels.

is a rare childhood-onset skin condition causing pitted, honeycomb-like facial scarring.

is prostate shrinkage that can affect urination and sexual function.

is shrinkage of one or both testicles, reducing hormone and sperm production.

is a neurodevelopmental condition causing inattention, hyperactivity, and impulsivity across settings.

is a milder form causing light pigmentation, frequent infections, bleeding, neuropathy.

is an inherited condition with fewer colon polyps and later-onset colorectal cancer.

is an inherited transthyretin amyloidosis causing late-onset cardiomyopathy and heart failure.

is an inherited transthyretin disorder with amyloid buildup damaging nerves, heart.

is an autism spectrum condition affecting social communication and behavior, variably.

is a benign breast duct growth with abnormal cells, raising cancer risk.

is a rare, intermediate-grade brain tumor of CSF-producing tissue causing fluid buildup.

is a rare, aggressive blood cancer with high white blood counts.

is rare aortic narrowing in atypical locations, causing high blood pressure.

is a rare genetic disorder causing defective dentin and early tooth loss.

is depression with mood improvement to good news, oversleeping, overeating, rejection sensitivity.

is a genetic disorder of dopamine transport, causing movement and developmental problems.

is a rare genetic disorder causing kidney Fanconi syndrome and neonatal hypoglycemia.

is a usually benign thyroid tumor with atypical cells, needing expert evaluation.

is a rare inherited disease causing enlarged organs, anemia, bone, neurologic problems.