ARHGAP29-related non-syndromic orofacial cleft

MONDO:1060132

Any orofacial cleft in which the cause of the disease is a mutation in the ARHGAP29 gene.

1 clinical trial for this condition and its sub-types, 0 tagged with ARHGAP29-related non-syndromic orofacial cleft 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.