| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Cyclopia is a congenital abnormality in which there is only one eye. That eye is centrally placed in the area normally occupied by the root of the nose. (Human Phenotype Ontology, HP_0009914) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0009914 |
| Similar Terms | |
| Downloads & Tools |
4 genes associated with the cyclopia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
