|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A type of hypothyroidism that results from a defect in the thyroid gland. (Human Phenotype Ontology, HP_0000832)|
|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.
|CTNS||cystinosin, lysosomal cystine transporter|