| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | any structural anomaly of the oral cavity (Mammalian Phenotype Ontology, MP_0000452) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D009056 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Mouth Abnormalities from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| PCSK5 | proprotein convertase subtilisin/kexin type 5 | 2.88009 |
