Human genes for Weaver syndrome
Weaver syndrome [DOID:14731]
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.
Synonyms: Weaver syndrome, DOID:14731, Weaver disease, Weaver disorder, Weaver syndromes ...
Linkouts: OMIM