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Summary Literature (0)
DOID:4154 - dentinogenesis imperfecta

Disease Ontology Definition:A tooth disease characterized by discolored, opalescent teeth that has_material_basis_in mutation in the DSPP gene on chromosome 4q22.

Synonyms:

Xenbase Genes : dspp

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018849 - dentinogenesis imperfecta


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), tooth disease (is_a)