FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Allan-Herndon-Dudley syndrome ID (Ontology) DOID:0050631 (Human Disease)
Definition A syndrome that has_material_basis_in mutation in the MCT8 gene on chromosome Xq13.
Also Known As "AHDS" ; "ALLAN-HERNDON SYNDROME"
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 Genes
 Allan-Herndon-Dudley syndrome       2
 for disease ribbon | Allan-Herndon-Dudley syndrome       2
 model of | Allan-Herndon-Dudley syndrome       2
Spanning Tree (Parents/Children)
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X-linked monogenic disease
 |__X-linked recessive disease__
disease                         |
 |__syndrome____________________|
                                Allan-Herndon-Dudley syndrome  2 rec.
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Is a X-linked recessive disease
syndrome
Part of
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Synonyms
  • "AHDS" EXACT OMO:0003012
    "ALLAN-HERNDON SYNDROME" EXACT
Secondary IDs
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GARD:5617
MESH:C537047
MIM:300523
ORDO:59