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Disease Ontology Browser
Weaver syndrome (DOID:14731)
Alliance: disease page
Synonyms: WEAVER-LIKE SYNDROME; Weaver-Williams syndrome
Alt IDs: OMIM:277590, MESH:C562443, UMLS_CUI:C0220765
Definition: 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.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
09/22/2022
MGI 6.21
The Jackson Laboratory