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

• MESH:C562769
• OMIM:274700

Ontology

Human Disease   ( DOID:0112187 )