| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An abnormality of thyroid physiology (HP:0002926) characterized by increased levels of thyroxine without evidence of clinical thyroid disease. (Human Phenotype Ontology, HP_0008247) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0008247 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the euthyroid hyperthyroxinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| DIO1 | deiodinase, iodothyronine, type I |
