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Echinobase
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:

Echinobase Genes :


MIM:
MIM:125490 - dentinogenesis imperfecta 1; dgi1
MIM:125500 - dentinogenesis imperfecta, shields type iii

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)