FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term thyroid dyshormonogenesis 4 ID (Ontology) DOID:0112188 (Human Disease)
Definition A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in IYD on chromosome 6q25.1.
Also Known As "deiodinase deficiency" ; "genetic defect in thyroid hormonogenesis 4" ; "iodotyrosine dehalogenase deficiency" (for all, see Synonyms field below)
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 Genes
 thyroid dyshormonogenesis 4       1
 for disease ribbon | thyroid dyshormonogenesis 4       1
 model of | thyroid dyshormonogenesis 4       1
Spanning Tree (Parents/Children)
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congenital hypothyroidism
 |__familial thyroid dyshormonogenesis__
autosomal genetic disease               |
 |__autosomal recessive disease_________|
                                        thyroid dyshormonogenesis 4  1 rec.
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Is a autosomal recessive disease
familial thyroid dyshormonogenesis
Part of
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Synonyms
  • "deiodinase deficiency" EXACT
    "genetic defect in thyroid hormonogenesis 4" EXACT
    "iodotyrosine dehalogenase deficiency" EXACT
    "TDH4" EXACT OMO:0003012
Secondary IDs
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MESH:C562770
MIM:274800