Meier-Gorlin syndrome 3

Definition

Any Meier-Gorlin syndrome in which the cause of the disease is a mutation in the ORC6 gene.

Also known as Meier-Gorlin syndrome 3, Meier-Gorlin syndrome caused by mutation in ORC6, Meier-Gorlin syndrome type 3, ORC6 Meier-Gorlin syndrome — per MONDO

Also identified as

• DOID 0080514 per MONDO
• OMIM 613803 per MONDO
• UMLS C3151113 per MONDO