Meckel syndrome, type 10

Definition

Any Meckel syndrome in which the cause of the disease is a mutation in the B9D2 gene.

Also known as B9D2 Meckel syndrome, meckel syndrome 10, Meckel syndrome caused by mutation in B9D2, Meckel syndrome, type 10 — per MONDO

Also identified as

• OMIM 614175 per MONDO
• UMLS C3280036 per MONDO