Search Ontology:
Human Disease

thyroid dyshormonogenesis 3

Term ID
DOID:0112187
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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