FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Brunet-Wagner neurodevelopmental syndrome ID (Ontology) DOID:0061126 (Human Disease)
Definition An autosomal recessive intellectual developmental disorder characterized by infantile hypotonia and severely impaired development affecting both motor and cognitive skills that has_material_basis_in homozygous or compound heterozygous mutation in the RBL2 gene on chromosome 16q12.
Also Known As "BRUWAG"
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 Brunet-Wagner neurodevelopmental syndrome       2      1
 for disease ribbon | Brunet-Wagner neurodevelopmental syndrome       2       --
 model of | Brunet-Wagner neurodevelopmental syndrome       2       --
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autosomal recessive disease
 |__autosomal recessive intellectual developmental disorder__
intellectual disability                                      |
 |__autosomal recessive intellectual developmental disorder__|
disease                                                      |
 |__syndrome_________________________________________________|
                                                             Brunet-Wagner neurodevelopmental syndrome  3 rec.
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Is a autosomal recessive intellectual developmental disorder
syndrome
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Synonyms
  • "BRUWAG" EXACT
Secondary IDs
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MIM:619690