congenital hypoparathyroidism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Deficiency of parathyroid hormone with congenital onset. (Human Phenotype Ontology, HP_0008198)
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1 genes associated with the congenital hypoparathyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
TBCE tubulin folding cofactor E