| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A type of dental dysplasia occurring in dentinogenesis imperfecta in which the pulp chambers are enlarged and there is a reduced amount of coronal dentin. (Human Phenotype Ontology, HP_0000694) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0000694 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the shell teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| DSPP | dentin sialophosphoprotein |
