Hay-Wells syndrome , HWS (skrót)
ankyloblepharon-ectodermal dysplasia-clefting syndrome

However, it was recently shown to the same disease as Hay-Wells syndrome.

Hay-Wells syndrome is inherited as an autosomal dominant trait.

Hay-Wells syndrome, Rapp-Hodgkin syndrome and EEC syndrome are all associated with TP63.

Hay-Wells syndrome (also known as AEC syndrome; see Naming) is one of at least 150 known types of ectodermal dysplasia.

Hay-Wells syndrome is autosomal dominant, caused by a missense mutation in the Sterile alpha motif (SAM) of the TP73L (p63) gene which encodes for a protein-protein interaction domain.

GeneReviews/NCBI/NIH/UW entry on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate Syndrome or AEC Syndrome, Hay-Wells Syndrome.