| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Nail that appears thin when viewed on end. (Human Phenotype Ontology, HP_0001816) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0001816 |
| Similar Terms | |
| Downloads & Tools |
6 genes associated with the thin nail phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ALOX12B | arachidonate 12-lipoxygenase, 12R type |
| EZH2 | enhancer of zeste 2 polycomb repressive complex 2 subunit |
| HRAS | Harvey rat sarcoma viral oncogene homolog |
| IFT122 | intraflagellar transport 122 |
| TRPS1 | trichorhinophalangeal syndrome I |
| WNT10A | wingless-type MMTV integration site family, member 10A |
