absent axillary hair Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of axillary hair. (Human Phenotype Ontology, HP_0002221)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002221
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4 genes associated with the absent axillary hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
APOE apolipoprotein E
GJB6 gap junction protein, beta 6, 30kDa
SNRPE small nuclear ribonucleoprotein polypeptide E
ZBTB20 zinc finger and BTB domain containing 20