| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Zlotogora-Ogur syndrome is an ectodermal dysplasia syndrome characterized by hair, skin and teeth anomalies, facial dysmophism with cleft lip and palate, cutaneous syndactyly and, in some cases, intellectual disability. (Orphanet Rare Disease Ontology, Orphanet_3253) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C536726 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Zlotogora-Ogur syndrome from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| PVRL1 | poliovirus receptor-related 1 (herpesvirus entry mediator C) | 2.88009 |
