Dentinogenesis imperfecta, shields type 3 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C538216
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Genes

1 genes/proteins associated with the disease Dentinogenesis imperfecta, shields type 3 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
DSPP dentin sialophosphoprotein 2.88009