trichorrhexis nodosa Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Trichorrhexis nodosa is the formation of nodes along the hair shaft through which breakage readily occurs. It is thus a focal defect in the hair fiber that is characterized by thickening or weak points (nodes) that cause the hair to break off easily. The result is defective, abnormally fragile hair. (Human Phenotype Ontology, HP_0009886)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009886
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Genes

4 genes associated with the trichorrhexis nodosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ASL argininosuccinate lyase
MPLKIP M-phase specific PLK1 interacting protein
SKIV2L superkiller viralicidic activity 2-like (S. cerevisiae)
TTC37 tetratricopeptide repeat domain 37