| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Axenfeld's anomaly is a bilateral disorder characterized by a prominent, anteriorly displaced Schwalbe's line (posterior embryotoxon) and peripheral iris strands which span the anterior chamber angle to attach to Schwalbe's line. (Human Phenotype Ontology, HP_0001492) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0001492 |
| Similar Terms | |
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2 genes associated with the axenfeld anomaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
