van den ende-gupta syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/600920
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Genes

1 genes associated with the van den ende-gupta syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SCARF2 scavenger receptor class F, member 2