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Disease Ontology Browser
Clark-Baraitser syndrome (DOID:0080234)
Alliance: disease page
Synonyms: autosomal dominant intellectual disability 49; autosomal dominant mental retardation 49; Baraitser syndrome; CLABARS
Alt IDs: OMIM:617752, MESH:C536208
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the TRIP12 gene on chromosome 2q36.

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
11/12/2024
MGI 6.24 		The Jackson Laboratory