is a genetic disorder causing copper buildup in liver, brain, eyes.

is a rare genetic condition affecting development, learning, growth, and hormones.

is a very rare genetic disorder affecting bones, joints, and connective tissue.

is a rare inherited immune disorder causing infections, eczema, and bleeding.

is a rare inflammatory illness causing fever, rash, and joint pain.

is a condition causing symptoms when someone stops or reduces a substance.

is a rare genetic condition affecting development, learning, behavior, and sometimes growth.

is a rare inherited disorder causing early diabetes and bone problems.

is a rare genetic condition causing developmental delay, seizures, and growth problems.

is a condition causing fast heart rhythms from an extra electrical pathway.

is a rare, usually benign tumor near the female reproductive tract.

is a rare cancer arising from Wolffian duct remnants, usually near ovaries.

is a rare, usually benign tumor from Wolffian duct remnants.

is a rare inherited disorder affecting insulin production, vision, hearing, and nerves.

is a rare genetic disorder causing childhood diabetes, vision and hearing loss.

is a rare genetic disorder causing diabetes, vision loss, and hearing loss.

is a rare inherited disorder causing diabetes, vision loss, and neurologic problems.

is a rare genetic condition causing diabetes, vision, hearing, and neurological problems.

is a rare infant-onset genetic disease causing fatty organ buildup.

is a rare inherited disorder causing hair loss, hormonal and neurological problems.

is a hair condition causing tightly curled, often fragile scalp hair.

is a rare patch of tightly curled, often lighter scalp hair.

is a rare genetic disorder with woolly hair and thickened palms, soles.

is a genetic disorder causing fragile bones, tooth defects, and skeletal changes.