Meckel syndrome, type 1

Any Meckel syndrome in which the cause of the disease is a mutation in the MKS1 gene.

Also known as: MKS1, MKS1 Meckel syndrome, Meckel syndrome caused by mutation in MKS1, Meckel syndrome, type 1, Meckel-Gruber syndrome, type 1, Dysencephalia Splanchnocystica, Dysencephalia splachnocystica, Gruber syndrome

38 clinical trials for this condition and its sub-types.