thyroid hypoplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Developmental hypoplasia of the thyroid gland. (Human Phenotype Ontology, HP_0005990)
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4 genes associated with the thyroid hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NKX2-5 NK2 homeobox 5
NSDHL NAD(P) dependent steroid dehydrogenase-like
PAX8 paired box 8
TSHR thyroid stimulating hormone receptor