Congenital Hypothyroidism Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A hypothyroidism that is present at birth. (Human Disease Ontology, DOID_0050328)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D003409
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Genes

4 genes/proteins associated with the disease Congenital Hypothyroidism from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
IGSF1 immunoglobulin superfamily, member 1 2.88009
DUOX2 dual oxidase 2 2.88009
TPO thyroid peroxidase 2.88009
TSHR thyroid stimulating hormone receptor 2.88009