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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)
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last database update
09/14/2021
MGI 6.17
The Jackson Laboratory