dentin dysplasia, type ii Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/125420
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Genes

1 genes associated with the dentin dysplasia, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
DSPP dentin sialophosphoprotein