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)
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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