| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Congenital absence (aplasia) of one or more limbs. (Human Phenotype Ontology, HP_0009827) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0009827 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the amelia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| WNT3 | wingless-type MMTV integration site family, member 3 |
