Summary Literature (0)

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: autosomal dominant intellectual disability 49, autosomal dominant mental retardation 49, Baraitser syndrome, CLABARS

Xenbase Genes : trip12

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0030914 - Clark-Baraitser syndrome

MIM:

MIM:617752 - CLARK-BARAITSER SYNDROME; CLABARS

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view