| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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 | https://www.disgenet.org/browser/0/1/0/C1863395 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the disease Acrobrachycephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| FGFR2 | fibroblast growth factor receptor 2 |
