is a rare congenital underdevelopment of the midface and nose.

involves difficulty coordinating both eyes, causing depth perception and focus problems.

is a detected biological difference without known symptoms or clinical features.

is a lack of vitamin B7 disrupting metabolism, skin, hair, nerves.

is a rare inherited brain disorder often improved with biotin treatment.

is a rare genetic brain disorder with episodic crises, seizures; biotin-thiamine responsive.

is a rare congenital foot variant with two talus parts, sometimes painful.

is a rare soft-tissue cancer near joints, involving two cell types.

is a mood disorder with depression and mania episodes affecting daily life.

is a mood disorder causing manic episodes and often depressive periods.

is a mood disorder with depression and hypomania, not full mania.

is immune-related lung inflammation (hypersensitivity pneumonitis) from inhaled bird proteins.

is a rare autoimmune eye disorder causing retinal inflammation and vision loss.

is a rare genetic neurodevelopmental disorder causing low muscle tone and delays.

is a genetic condition causing skin bumps, lung cysts, and kidney tumors.

is a rare noncancerous (benign) smooth muscle tumor, usually in the uterus.

is a rare inherited disorder causing brittle twisted hair and hearing loss.

is a rare, severe malaria complication with dark urine, anemia, kidney injury.

is a rare bladder cancer from gland-forming lining cells.

is a noncancerous bladder tumor that may cause urinary symptoms.

is a hard mineral deposit in the bladder causing urinary symptoms.

is a bladder lining cancer, often causing blood in urine.

is a high-grade, noninvasive cancer of the bladder lining.

is a rare bladder cancer subtype with clear cells, often aggressive.