Temporal Hypotrichosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Reduced or lacking hair growth in the temporal region (i.e., around the temples on the side of the skull). (Human Phenotype Ontology, HP_0004524)
External Link https://www.disgenet.org/browser/0/1/0/C4025316
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Genes

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

Symbol Name
GJB2 gap junction protein, beta 2, 26kDa
KRT85 keratin 85, type II
SOX11 SRY (sex determining region Y)-box 11