X-linked Opitz G/BBB syndrome

X-linked Opitz G/BBB syndrome is a rare genetic condition. It is defined as the X-linked form of Opitz G/BBB syndrome and is associated with changes in specific genes, such as MID1. The condition is inherited in an X-linked pattern, which means the gene change is passed through the X chromosome. This can result in a range of features that may vary from person to person.

Information about symptoms is currently limited for this condition.

This condition is linked to changes in the MID1 gene on the X chromosome. Because it follows an X-linked inheritance pattern, the syndrome is more frequently observed in males, while females may serve as carriers. The specific genetic change in MID1 disrupts normal development, though details about how it causes the range of symptoms are still being studied. Associated genes include MID1.