Thyroglossal Cyst Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	An abnormality of the thyroid gland owing to the presence of a fibrous cyst resulting from the persistence of the thyroglossal duct. (Human Phenotype Ontology, HP_0010518)
External Link	https://www.disgenet.org/browser/0/1/0/C0040124
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Genes

7 genes associated with the disease Thyroglossal Cyst in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
ATRX	alpha thalassemia/mental retardation syndrome X-linked
CDKN2A	cyclin-dependent kinase inhibitor 2A
CHPT1	choline phosphotransferase 1
DHDDS	dehydrodolichyl diphosphate synthase
NT5E	5'-nucleotidase, ecto (CD73)
SMUG1	single-strand-selective monofunctional uracil-DNA glycosylase 1
TEF	thyrotrophic embryonic factor