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Meckel syndrome, type 8

MONDO:0013482

Any Meckel syndrome in which the cause of the disease is a mutation in the TCTN2 gene.

Also known as: MKS8, Meckel syndrome caused by mutation in TCTN2, Meckel syndrome, type 8, TCTN2 Meckel syndrome, Meckel syndrome 8

0 clinical trials for this condition and its sub-types, 0 tagged with Meckel syndrome, type 8 itself.

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