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Disease Ontology Browser
Coffin-Siris syndrome 3 (DOID:0070045)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 15; CSS3; MRD15
Alt IDs: OMIM:614608
Definition: A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of the SMARCB1 gene on chromosome 22q11.23.

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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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory