FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term female-restricted Wieacker-Wolff syndrome ID (Ontology) DOID:0061015 (Human Disease)
Definition A syndromic X-linked intellectual disability that has_material_basis_in heterozygous mutation in the ZC4H2 gene on chromosome Xq11.
Also Known As "WRWFFR"
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DO.org
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 Genes
 female-restricted Wieacker-Wolff syndrome       1
 for disease ribbon | female-restricted Wieacker-Wolff syndrome       1
 model of | female-restricted Wieacker-Wolff syndrome       1
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__syndromic X-linked intellectual disability__
 |__X-linked dominant disease___________________|
syndromic intellectual disability               |
 |__syndromic X-linked intellectual disability__|
                                                female-restricted Wieacker-Wolff syndrome  1 rec.
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Is a syndromic X-linked intellectual disability
X-linked dominant disease
Part of
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Synonyms
  • "WRWFFR" EXACT OMO:0003012
Secondary IDs
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MIM:301041