Meckel syndrome, type 6

MONDO:0012848

Any Meckel syndrome in which the cause of the disease is a mutation in the CC2D2A gene.

Also known as: CC2D2A Meckel syndrome, MKS6, Meckel syndrome caused by mutation in CC2D2A, Meckel syndrome, type 6, Meckel syndrome 6

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

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