primary hypothyroidism Gene Set

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

Genes

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