Seckel syndrome 6

MONDO:0013871

Any Seckel syndrome in which the cause of the disease is a mutation in the CEP63 gene.

Also known as: CEP63 Seckel syndrome, SCKL6, Seckel syndrome 6, Seckel syndrome caused by mutation in CEP63, Seckel syndrome type 6

0 clinical trials for this condition and its sub-types, 0 tagged with Seckel syndrome 6 itself.

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