|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Van den Ende-Gupta syndrome is a very rare syndrome characterized by blepharophimosis, arachnodactyly, joint contractures, and characteristic dysmorphic features. (Orphanet Rare Disease Ontology, Orphanet_2460)|
|Downloads & Tools|
1 genes associated with the van den ende-gupta syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
|SCARF2||scavenger receptor class F, member 2|