congenital hypothyroidism Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A hypothyroidism that is present at birth. (Human Disease Ontology, DOID_0050328)
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Genes

2 genes associated with the disease congenital hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
TSHR thyroid stimulating hormone receptor
TTF1 transcription termination factor, RNA polymerase I