| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Incomplete fusion of the chin, resulting from a developmental defect and manifesting as a midline cleft or fissure of the chin. (Human Phenotype Ontology, HP_0011323) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0011323 |
| Similar Terms | |
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2 genes associated with the cleft of chin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
