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dentinogenesis imperfecta

  1. Record numberd003811
    Date06.06.2025
    TypeM - MESH
    Topical termdentinogenesis imperfecta
    Other termEnglish (Pseudonym) Hereditary Opalescent Dentin
    Slovak (Pseudonym) dentinogenesis imperfecta hereditaria
    See also(Skutočné meno) osteogenesis imperfecta
    (Later heading) osteogenesis imperfecta
    UDCC07.650.800.270C07.793.700.270C16.131.850.800.270
    NoteAn autosomal dominant disorder of tooth development characterized by opalescent dentin resulting in discoloration of the teeth. The dentin develops poorly with low mineral content while the pulp canal is obliterated.
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Number of the records: 1  

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