is an inherited disorder that affects liver glycogen breakdown and blood sugar.

is a rare inherited disorder affecting glycogen breakdown, mainly in muscles.

is a rare inherited muscle disease causing exercise intolerance, cramps, and anemia.

is a rare inherited disorder affecting how the body stores glycogen.

is an inherited disorder causing low blood sugar and thickened heart muscle.

is a rare inherited disorder causing glycogen buildup and severe heart disease.

is a rare cancer whose cells contain unusually high amounts of glycogen.

is a rare type of breast cancer with cells containing glycogen.

is a rare inherited disorder causing harmful buildup of sugar-protein compounds.

is a rare genetic condition disrupting GPI anchors, causing developmental delays.

is a rare inherited lysosomal disorder causing progressive brain and body damage.

is a rare inherited disorder causing severe brain and body problems.

is an inherited disorder causing harmful buildup that damages the brain.

is a rare inherited disorder that gradually affects movement, speech, and thinking.

is a rare inherited disorder that damages nerve cells in the brain.

is a rare inherited disorder causing harmful fat buildup in nerve cells.

is a rare inherited disorder causing early seizures and severe neurodevelopmental impairment.

is an inherited muscle disease causing progressive proximal limb weakness.

is a rare genetic condition that affects development and body systems.

is a genetic brain disorder causing developmental delays, seizures, and movement problems.

is a rare inherited bone disorder causing fragile bones and jaw lesions.

is a rare parasitic infection usually caused by eating raw seafood.

is a rare genetic condition causing developmental delays and abnormal heart rhythms.

is a rare genetic muscle disorder causing progressive weakness, starting in feet.