thyroid agenesis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The congenital absence of the thyroid gland. (Human Phenotype Ontology, HP_0008191)
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2 genes associated with the thyroid agenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FOXE1 forkhead box E1
PAX8 paired box 8