|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Dentin dysplasia type II (DD-II) is a rare mild form of dentin dysplasia (DD, see this term) characterized by normal tooth roots but abnormal primary dentition. (Orphanet Rare Disease Ontology, Orphanet_99791)|
|Downloads & Tools|
1 genes associated with the dentin dysplasia, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.