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- B2e5f257ca809491aad9ca1ab5e4747fa hasDbXref "Orphanet:167759" @default.
- B2e5f257ca809491aad9ca1ab5e4747fa type Axiom @default.
- B2e5f257ca809491aad9ca1ab5e4747fa annotatedProperty IAO_0000115 @default.
- B2e5f257ca809491aad9ca1ab5e4747fa annotatedSource MONDO_0015668 @default.
- B2e5f257ca809491aad9ca1ab5e4747fa annotatedTarget "The hereditary dentin disorders, dentinogenesis imperfecta (DGI) and dentin dysplasia (DD), comprise a group of conditions characterized by abnormal dentin structure affecting either the primary or both the primary and secondary dentitions." @default.