Mucolipidosis I (ML I), or sialidosis, is a rare, inherited disorder in which genetic variations disrupt the normal activity of lysosomes in human cells.
Mucolipidosis II (ML II), or I-cell disease, is a rare, inherited disorder in which genetic variations disrupt the normal activity of lysosomes in human cells.
Mitochondrial disease is not a single disorder but an umbrella term for dozens of individual disorders in which the body’s cells have problems producing energy.