| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A kind of congenital defect of the anterior abdominal wall in which the intestines are evident through the thin, lax, and protruding abdominal wall in affected infants. (Human Phenotype Ontology, HP_0004392) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0004392 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the prune belly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CHRM3 | cholinergic receptor, muscarinic 3 |
