| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A congenital malformation characterized by the union or approximation of the ears in front of the neck, often accompanied by the absence or defective development of the lower jaw. (Human Phenotype Ontology, HP_0100663) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0100663 |
| Similar Terms | |
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2 genes associated with the synotia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
