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