goiter Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Enlargement of the THYROID GLAND that may increase from about 20 grams to hundreds of grams in human adults. Goiter is observed in individuals with normal thyroid function (euthyroidism), thyroid deficiency ( HYPOTHYROIDISM), or hormone overproduction ( HYPERTHYROIDISM). Goiter may be congenital or acquired, sporadic or endemic ( GOITER, ENDEMIC). (Experimental Factor Ontology, EFO_0004283)
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Genes

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

Symbol Name
CAPZB capping protein (actin filament) muscle Z-line, beta
FAM227B family with sequence similarity 227, member B
FGF7 fibroblast growth factor 7