|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Dentinogenesis imperfecta type 3 (DGI-3) is a rare, severe form of dentinogenesis imperfecta (DGI, see this term) characterized by opalescent primary and permanent teeth, marked attrition, large pulp chambers, multiple pulp exposure and shell teeth radiographically (i.e. teeth which appear hollow due to dentin hypotrophy). (Orphanet Rare Disease Ontology, Orphanet_166265)|
|Downloads & Tools|
1 genes/proteins associated with the disease Dentinogenesis imperfecta, shields type 3 from the curated CTD Gene-Disease Associations dataset.