abnormal hair whorl Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal hair whorl (that is, a patch of hair growing in the opposite direction of the rest of the hair). (Human Phenotype Ontology, HP_0010721)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010721
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8 genes associated with the abnormal hair whorl phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CREBBP CREB binding protein
MED12 mediator complex subunit 12
NDN necdin, melanoma antigen (MAGE) family member
SNRPN small nuclear ribonucleoprotein polypeptide N
STAMBP STAM binding protein
UBE2A ubiquitin-conjugating enzyme E2A
UBR1 ubiquitin protein ligase E3 component n-recognin 1
WRN Werner syndrome, RecQ helicase-like