FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Clark-Baraitser syndrome ID (Ontology) DOID:0080234 (Human Disease)
Definition An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the TRIP12 gene on chromosome 2q36.
Also Known As "autosomal dominant intellectual disability 49" ; "autosomal dominant mental retardation 49" ; "Baraitser syndrome" (for all, see Synonyms field below)
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 Genes
 Clark-Baraitser syndrome       1
 for disease ribbon | Clark-Baraitser syndrome       1
 model of | Clark-Baraitser syndrome       1
Spanning Tree (Parents/Children)
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autosomal dominant disease__
intellectual disability_____|
                            autosomal dominant intellectual developmental disorder
                             |__Clark-Baraitser syndrome  1 rec.
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Is a autosomal dominant intellectual developmental disorder
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Synonyms
  • "autosomal dominant intellectual disability 49" EXACT
    "autosomal dominant mental retardation 49" EXACT
    "Baraitser syndrome" EXACT
    "CLABARS" EXACT OMO:0003012
Secondary IDs
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GARD:13584
MESH:C536208
MIM:617752