frontal balding Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of hair in the anterior midline and/or parietal areas. (Human Phenotype Ontology, HP_0002292)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002292
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Genes

2 genes associated with the frontal balding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CNBP CCHC-type zinc finger, nucleic acid binding protein
DMPK dystrophia myotonica-protein kinase