| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Any abnormality of dentin. (Human Phenotype Ontology, HP_0010299) |
| External Link | https://www.disgenet.org/browser/0/1/0/C4021299 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the disease Abnormality Of Dentin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CDH11 | cadherin 11, type 2, OB-cadherin (osteoblast) |
