| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A type of hypothyroidism that results from a defect in the thyroid gland. (Human Phenotype Ontology, HP_0000832) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0000832 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the primary hypothyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CTNS | cystinosin, lysosomal cystine transporter |
