is a common superficial skin infection causing brown, mildly itchy patches.

is a rare inherited disorder affecting how the body processes galactose.

is a rare skin disorder causing widespread redness and peeling.

is a rare skin disorder causing red patches and thickened skin.

is a rare inherited skin disorder causing target-like red patches.

is a rare inherited skin disorder causing red patches and thickened skin.

is a rare inherited skin disorder causing red patches and thickened skin.

is a rare inherited skin disorder with migratory redness and thickened plaques.

is a rare inherited skin disorder causing changing redness and thickened skin.

is a rare inherited skin disorder causing shifting red, thickened patches.

is a rare inherited skin disorder causing changing redness and thickened patches.

is a rare inherited skin disorder causing red patches and thickened skin.

is a rare inherited disorder causing shifting red patches and thickened skin.

is a rare inherited condition causing red, thickened skin and heart disease.

is a rare blood cancer affecting immature red and white blood cells.

causes burning pain, warmth, and redness, usually in the hands and feet.

is a rare porphyria linked to blood cancers, causing severe sun sensitivity.

is a rare condition causing too many red blood cells.

is a rare cancer that starts in mucus glands of the esophagus.

is a rare esophageal cancer containing both glandular and squamous cells.

is a birth defect where the esophagus does not form properly.

is a birth defect where the food pipe and windpipe form abnormally.

is a rare, aggressive cancer arising from cells lining the esophagus.

is a cancer of the esophagus causing swallowing difficulty and chest pain.