OBO ID: DOID:0112189
Term Name: thyroid dyshormonogenesis 6 Search Ontology:
Synonyms:
  • genetic defect in thyroid hormonogenesis 6
  • TDH6
Definition: A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in DUOX2 on chromosome 15q21.1. https://pubmed.ncbi.nlm.nih.gov/12110737/
References:
Ontology: Human Disease   ( DOID:0112189 )
Relationships
is a type of:
OTHER thyroid dyshormonogenesis 6 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DUOX1 Thyroid dyshormonogenesis 6 607200
DUOX2 Thyroid dyshormonogenesis 6 607200
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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