FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term X-linked VACTERL association ID (Ontology) DOID:0111766 (Human Disease)
Definition A VACTERL association that has_material_basis_in mutation in the ZIC3 gene on chromosome Xq26.3 or the FANCB gene on chromosome Xp22.2.
Also Known As "VACTERL association, X-linked with or without hydrocephalus" ; "VACTERLX"
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DO.org
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 Genes
 X-linked VACTERL association       1
 for disease ribbon | X-linked VACTERL association       1
 model of | X-linked VACTERL association       1
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__X-linked recessive disease__
syndrome                        |
 |__VACTERL association_________|
                                X-linked VACTERL association  1 rec.
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Is a X-linked recessive disease
VACTERL association
Part of
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Synonyms
  • "VACTERL association, X-linked with or without hydrocephalus" EXACT
    "VACTERLX" EXACT OMO:0003012
Secondary IDs
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GARD:8498
MIM:314390