is a rare inherited disorder affecting muscles, bones, and sometimes behavior.

is a rare disorder with myopathy, Paget bone disease, and frontotemporal dementia.

is a slowly progressive muscle disease causing weakness and trouble swallowing.

is an eye infection caused by chlamydia, leading to redness and discharge.

is a rare muscle disease causing weakness and sometimes trouble swallowing.

is a rare liver condition with incomplete scarring and possible portal hypertension.

is a rare genetic condition affecting skin, teeth, hair, eyes, nerves.

is a rare disorder where immune cells build up, usually in skin.

is an early, mild form of leprosy with subtle skin changes.

is an allergic reaction to Indian plum, causing symptoms after exposure.

is an allergy to Indian prawns that can cause serious reactions.

is a bacterial infection spread by ticks that causes fever and rash.

is a slow-growing B-cell cancer affecting infection-fighting white blood cells.

is a slow-growing blood cancer that may not cause symptoms initially.

is a slow-growing skin lymphoma involving B cells, usually with excellent outlook.

is a slow-growing skin lymphoma involving immune T cells.

is a usually slow-growing mast cell disorder causing allergy-like symptoms.

is a rare birth defect pattern linked to indomethacin exposure during pregnancy.

is a rare epilepsy syndrome causing seizures and developmental problems in infancy.

is a severe breathing problem causing low oxygen in sick infants.

is a rare illness in babies caused by botulinum toxin.

is a rare, aggressive brain tumor affecting one side of infants' brains.

is a breathing pause in infants that may need urgent evaluation.

is a rare childhood brain disorder affecting movement, speech, and development.