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DOID:0080234 - Clark-Baraitser syndrome
Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the TRIP12 gene on chromosome 2q36.
Synonyms: Baraitser syndrome, CLABARS, autosomal dominant intellectual disability 49, autosomal dominant mental retardation 49,
Xenbase Genes : trip12
MONDO:0030914 - Clark-Baraitser syndrome |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee