congenital goiter Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An enlargement of the thyroid gland with congenital onset. (Human Phenotype Ontology, HP_0008251)
External Link
Similar Terms
Downloads & Tools


1 genes associated with the congenital goiter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NKX2-1 NK2 homeobox 1