About   Help   FAQ
Disease Ontology Browser
thyroid dyshormonogenesis 3 (DOID:0112187)
Alliance: disease page
Synonyms: genetic defect in thyroid hormonogenesis 3; TDH3
Alt IDs: OMIM:274700, MESH:C562769
Definition: A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in TG on chromosome 8q24.22.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
MGI 6.23
The Jackson Laboratory