| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An abnormality of head shape characterized by the presence of a short, wide head as well as a pointy or conical form of the top of the head owing to premature closure of the coronal and lambdoid sutures. (Human Phenotype Ontology, HP_0004487) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0004487 |
| Similar Terms | |
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1 genes associated with the acrobrachycephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| FGFR2 | fibroblast growth factor receptor 2 |
