Meckel syndrome, type 11

Definition

Any Meckel syndrome in which the cause of the disease is a mutation in the TMEM231 gene.

Also known as meckel syndrome 11, Meckel syndrome caused by mutation in TMEM231, Meckel syndrome, type 11, TMEM231 Meckel syndrome — per MONDO

Also identified as

• OMIM 615397 per MONDO
• UMLS C3809352 per MONDO