Meckel syndrome type 11 is an autosomal recessive disorder caused by mutations in the TMEM231 gene.
Meckel syndrome | ||||
Meckel syndrome 02 | ||||
Meckel syndrome 03 | ||||
Meckel syndrome 05 | ||||
Meckel syndrome 06 | ||||
Meckel syndrome 08 | ||||
Meckel syndrome 09 | ||||
Meckel syndrome 10 | ||||
Meckel syndrome 11 | ||||
TMEM231 | ||||
Meckel syndrome 13 | ||||
1. |
Shaheen R et al. (2013) Mutations in TMEM231 cause Meckel-Gruber syndrome. |
2. |
OMIM.ORG article Omim 615397 |