Lowe Disease, also known as Oculocerebrorenal Syndrome, is a rare genetic disorder. It affects various organs, including the eyes, brain, and kidneys. Although there are no direct synonyms for Lowe Disease, it can also be referred to as Dent Disease Type 2 or OCRL Syndrome, both of which are alternative names to describe this condition. This condition primarily affects males and is characterized by developmental delays, vision impairments, kidney dysfunction, and intellectual disabilities. It is essential for healthcare professionals and families to be aware of these alternate names to ensure accurate diagnosis and access to appropriate treatment for individuals affected by Lowe Disease.