FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term White-Sutton syndrome ID (Ontology) DOID:0070067 (Human Disease)
Definition An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the POGZ gene on chromosome 1q21.3.
Also Known As "autosomal dominant mental retardation 37" ; "MRD37" ; "WHSUS"
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DO.org
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 White-Sutton syndrome       1      1
 for disease ribbon | White-Sutton syndrome       1       --
 model of | White-Sutton syndrome       1       --
Spanning Tree (Parents/Children)
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autosomal dominant disease__
intellectual disability_____|
                            autosomal dominant intellectual developmental disorder
                             |__White-Sutton syndrome  2 rec.
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Is a autosomal dominant intellectual developmental disorder
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Synonyms
  • "autosomal dominant mental retardation 37" EXACT
    "MRD37" EXACT OMO:0003012
    "WHSUS" EXACT OMO:0003012
Secondary IDs
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MIM:616364