|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormality of fascia. (Human Phenotype Ontology, HP_0100536)|
|Downloads & Tools|
1 genes associated with the abnormality of the fascia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|TNFRSF1A||tumor necrosis factor receptor superfamily, member 1A|