Hypothalamic Hypothyroidism Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of hypothyroidism that results from a defect in thyrotropin-releasing hormone activity. (Human Phenotype Ontology, HP_0008237)
External Link https://www.disgenet.org/browser/0/1/0/C0220998
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Genes

5 genes associated with the disease Hypothalamic Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
NF2 neurofibromin 2 (merlin)
PDGFB platelet-derived growth factor beta polypeptide
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
SUFU suppressor of fused homolog (Drosophila)
TRH thyrotropin-releasing hormone