Version: 8.0.0
Date: Tue Jan 28 2025
thyroid dyshormonogenesis 6
DOID:0112189
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

thyroid dyshormonogenesis 6

Definition
A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in DUOX2 on chromosome 15q21.1.
Synonyms
  • genetic defect in thyroid hormonogenesis 6
  • TDH6
Cross References
Parent Terms
Child Terms
None
Sources of Associations

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