DENTIN DYSPLASIA, TYPE II Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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://ctdbase.org/detail.go?type=disease&acc=OMIM:125420
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Genes

1 genes/proteins associated with the disease DENTIN DYSPLASIA, TYPE II from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
DSPP dentin sialophosphoprotein 2.88009