Mirhosseini-Holmes-Walton Syndrome is a rare genetic disorder that affects the development of the eyes, teeth, and craniofacial features. Due to its rarity, there are currently no established synonyms for this condition. However, it is also known as "Holmes Syndrome" and "Walton Syndrome" as it was named after the researchers who first identified and described the condition. Other medical terms that may be associated with this syndrome include "oculodentodigital dysplasia" and "ODDD." These terms describe the specific features of the syndrome, including abnormalities in the eyes, teeth, and bone structure. Early diagnosis and management of the symptoms can help improve the quality of life of individuals affected by this condition.