OBO ID: DOID:0112187
Term Name: thyroid dyshormonogenesis 3 Search Ontology:
Synonyms:
  • genetic defect in thyroid hormonogenesis 3
  • TDH3
Definition: A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in TG on chromosome 8q24.22. https://pubmed.ncbi.nlm.nih.gov/17244789/
References:
Ontology: Human Disease   ( DOID:0112187 )
Relationships
is a type of:
OTHER thyroid dyshormonogenesis 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TG Thyroid dyshormonogenesis 3 274700
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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