Seckel syndrome 5

MONDO:0013443

Any Seckel syndrome in which the cause of the disease is a mutation in the CEP152 gene.

Also known as: CEP152 Seckel syndrome, SCKL5, Seckel syndrome 5, Seckel syndrome caused by mutation in CEP152, Seckel syndrome type 5

0 clinical trials for this condition and its sub-types, 0 tagged with Seckel syndrome 5 itself.

Where it sits in the disease tree

Part of

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.