|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Hand-foot-genital syndrome (HFGS) is a very rare multiple congenital abnormality syndrome characterized by distal limb malformations and urogenital defects. (Orphanet Rare Disease Ontology, Orphanet_2438)|
|Downloads & Tools|
1 genes associated with the hand-foot-uterus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.