| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Absence of the fibula. (Human Phenotype Ontology, HP_0002990) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0002990 |
| Similar Terms | |
| Downloads & Tools |
8 genes associated with the fibular aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| AMER1 | APC membrane recruitment protein 1 |
| BMPR1B | bone morphogenetic protein receptor, type IB |
| FLNB | filamin B, beta |
| GDF5 | growth differentiation factor 5 |
| LMBR1 | limb development membrane protein 1 |
| RBM8A | RNA binding motif protein 8A |
| TBX15 | T-box 15 |
| WNT7A | wingless-type MMTV integration site family, member 7A |
