| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Rosselli-Gulienetti syndrome is a type of ectodermal dysplasia characterized by anhidrosis, hypotrichosis, cleft and lip palate, microdontia and syndactyly. (Orphanet Rare Disease Ontology, Orphanet_90339) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C563117 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Rosselli-Gulienetti Syndrome from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| PVRL1 | poliovirus receptor-related 1 (herpesvirus entry mediator C) | 2.88009 |
