| 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 |
| Similar Terms | |
| Downloads & Tools |
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 |
