thyroid dyshormonogenesis 3
Ontology Term:
Status:
Live
Synonym:
TDH3
genetic defect in thyroid hormonogenesis 3
genetic defect in thyroid hormonogenesis 3
Type:
Mapping to OMIM ID:
Comparative Info:
Learn more about this disease from studies in other model systems at the 
WormBase ID:
DOID:0112187
A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in TG on chromosome 8q24.22.
Child:
Associations based on experimental data:
Disease relevant gene:
Automatic gene association:
1 Inferred automatically: Inferred by orthology to human genes with OMIM annotation
