Human genes for Weyers acrofacial dysostosis
Weyers acrofacial dysostosis [DOID:0111571]
An acrofacial dysostosis characterized by dental anomalies, nail dystrophy, postaxial polydactyly, and mild short stature that has_material_basis_in heterozygous mutation in the genes EVC2 or EVC on chromosome 4p16.2.
Synonyms: Weyers acrofacial dysostosis, DOID:0111571, Weyers acrofacial dysostosises, acrofacial dysostosis, Weyers type, Curry-Hall syndrome ...