is a rare inherited macular dystrophy causing progressive central vision loss.

is a rare, slow-growing noncancerous soft-tissue tumor that may recur.

is a harmless skin nerve-sheath tumor (schwannoma), usually solitary, painless, slow-growing.

is a rare, noncancerous sweat gland tumor causing tender breast skin bumps.

is a noncancerous growth in salivary glands, usually slow-growing and painless.

is long-term high blood pressure without a clear secondary cause.

is a noncancerous (benign) pancreatic tumor from enzyme-producing tissue, often found incidentally.

is an inherited condition causing microscopic blood in urine (hematuria), usually harmless.

is a genetic seizure disorder in infancy, usually resolving by age 2.

is a genetic condition causing brief infant seizures that resolve by toddlerhood.

is an inherited infant epilepsy; seizures are brief and usually self-limited.

causes brief, recurrent infant seizures in healthy babies, often resolving by toddlerhood.

causes brief, self-limited seizures in infancy, often running in families.

causes genetic, brief, self-limited infant seizures with normal development.

is a genetic epilepsy causing self-limited infant seizures with normal development.

is an inherited focal epilepsy causing temporal-lobe seizures with generally good outlook.

is a genetic neonatal epilepsy causing brief seizures, often resolving spontaneously.

is a hereditary epilepsy with brief neonatal-infantile seizures and good prognosis.

is a rare, usually noncancerous tumor of the chest lining (pleura).

is a teen-onset epilepsy causing focal seizures, often remitting by adulthood.

is a usually noncancerous bone tumor near joints causing pain and swelling.

is a genetic, nonprogressive movement disorder causing early-onset chorea.

is kidney damage from long-term high blood pressure, often slowly progressive.

are short newborn seizures of unknown cause, usually resolve by infancy.