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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008191
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Genes

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