About   Help   FAQ
Disease Ontology Browser
White-Sutton syndrome (DOID:0070067)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 37; MRD37; WHSUS
Alt IDs: OMIM:616364
Definition: An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of POGZ on chromosome 1q21.3.

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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.17
The Jackson Laboratory