| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An autosomal recessive disease that is characterised by severe reduction or absence of the fibula and complex brachydactyly. (Human Disease Ontology, DOID_0050790) |
| External Link | https://www.disgenet.org/browser/0/1/0/C1856738 |
| Similar Terms | |
| Downloads & Tools |
3 genes associated with the disease Fibular Hypoplasia And Complex Brachydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
