congenital hypothyroidism Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
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

14 genes involed in the disease congenital hypothyroidism from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
DUOX2 dual oxidase 2
DUOXA2 dual oxidase maturation factor 2
GLIS3 GLIS family zinc finger 3
IGSF1 immunoglobulin superfamily, member 1
IYD iodotyrosine deiodinase
NKX2-1 NK2 homeobox 1
NKX2-5 NK2 homeobox 5
PAX8 paired box 8
SLC5A5 solute carrier family 5 (sodium/iodide cotransporter), member 5
TG thyroglobulin
THRA thyroid hormone receptor, alpha
TPO thyroid peroxidase
TSHB thyroid stimulating hormone, beta
TSHR thyroid stimulating hormone receptor