is a rare form of diabetes that starts in early infancy.

is a rare genetic syndrome causing newborn diabetes and multiple organ problems.

is a rare inherited disorder causing severe brain, heart, and breathing problems.

is a group of early-life seizure disorders affecting newborn babies.

is a rare inherited disorder causing seizures and severe early brain dysfunction.

is a rare genetic disorder causing glycine buildup and severe brain symptoms.

is a rare newborn liver disease with severe iron buildup.

is brain damage from low oxygen or blood flow around birth.

is a rare inherited disorder causing scaly skin and bile duct scarring.

is a breast infection in newborns causing swelling, redness, and tenderness.

is a rare inherited disorder causing severe skin inflammation and bowel disease.

is a rare inherited liver disorder causing cholestasis in newborns.

is newborn exposure to excess iodine, which can temporarily affect thyroid function.

is common newborn yellowing of the skin and eyes from bilirubin buildup.

is a rare blood cancer diagnosed in newborns and young infants.

is a rare autoimmune condition affecting some newborns of mothers with antibodies.

is a rare, severe form of Marfan syndrome affecting newborns.

is a temporary muscle weakness disorder in newborns caused by maternal antibodies.

is a rare genetic disorder causing unusually dense, fragile bones in newborns.

is a rare genetic epilepsy causing severe seizures in newborns.

is severe breathing difficulty in newborns needing urgent medical support.

is a rare newborn condition causing hard, tight skin and illness.

is a rare genetic disorder causing life-threatening heart and lung failure.

is a rare genetic disorder causing life-threatening high calcium (hypercalcemia) in newborns.