Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

Meckel syndrome 11

Meckel syndrome type 11 is an autosomal recessive disorder caused by mutations in the TMEM231 gene.

Systematic

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

References:

1.

Shaheen R et. al. (2013) Mutations in TMEM231 cause Meckel-Gruber syndrome.

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Update: Oct. 11, 2018