Holoprosencephaly 2

MONDO:0007999

A rare disorder characterized by the partial separation of the cerebral hemispheres. It is associated with mutations in the SIX3 gene.

Also known as: HPE2, SIX3 holoprosencephaly, holoprosencephaly 2, holoprosencephaly caused by mutation in SIX3, holoprosencephaly type 2

0 clinical trials for this condition and its sub-types, 0 tagged with Holoprosencephaly 2 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.