Summary

46 Craniofrontonasal dysplasia is a rare genetic condition caused by a change (mutation) in the efnb1 gene.  main features of this condition include widely spaced eyes (hypertelorism), broad-tipped nose, broad head (brachycephaly), prominent forehead (frontal bossing), asymmetry of facial features, and/or crossed eyes (strabismus). females affected with this condition generally have more symptoms than affected males.  treatment may include surgery to correct the shape of the skull or to adjust the facial features associated with this condition

All SNPs

Disease Hierarchy

Processes Associated With Trait

Pathways Associated With Trait

Symptoms Associated With Trait