| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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 | https://www.disgenet.org/browser/0/1/0/C2981132 |
| Similar Terms | |
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5 genes associated with the disease Shell Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
