autosomal dominant disease Weaver syndrome OMIM mapping confirmed by DO. [LS]. GARD:7878 GARD:5545 UMLS_CUI:C0220765 A syndrome that is characterized by prenatal and postnatal overgrowth, accelerated osseous maturation, characteristic craniofacial appearance, and developmental delay and has_material_basis_in heterozygous mutation in the EZH2 gene on chromosome 7q36. OMIM:277590 DOID:14731 disease_ontology MESH:C562443 WEAVER-LIKE SYNDROME Weaver-Williams syndrome syndrome