| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An abdominal hernia that occurs at a site of weakness in the abdominal wall resulting from an incompletely-healed surgical wound. (Human Phenotype Ontology, HP_0004872) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0004872 |
| Similar Terms | |
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1 genes associated with the incisional hernia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| FBN1 | fibrillin 1 |
