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Disease Ontology Browser
Coffin-Siris syndrome 2 (DOID:0070044)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 14; CSS2; MRD14
Alt IDs: OMIM:614607
Definition: A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of the ARID1A gene on chromosome 1p36.11.

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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
12/17/2024
MGI 6.24 		The Jackson Laboratory