| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Missing ulna bone associated with congenital failure of development. (Human Phenotype Ontology, HP_0003982) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0003982 |
| Similar Terms | |
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4 genes associated with the absent ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
