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367461002: Dentinogenesis imperfecta (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2002. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    492191017 Dentinogenesis imperfecta (disorder) en Synonym Inactive Only initial character case insensitive SNOMED CT core module
    776167012 Dentinogenesis imperfecta [dup] (disorder) en Fully specified name Inactive Only initial character case insensitive SNOMED CT core module
    2670864018 Dentinogenesis imperfecta [dup] en Synonym Inactive Only initial character case insensitive SNOMED CT core module
    2736349010 Dentinogenesis imperfecta (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    2771347018 Dentinogenesis imperfecta en Synonym Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Dentinogenesis imperfecta Is a Hereditary or idiopathic disturbance of tooth structure false Inferred relationship Existential restriction modifier
    Dentinogenesis imperfecta Finding site Jaw region structure false Inferred relationship Existential restriction modifier
    Dentinogenesis imperfecta Finding site Tooth structure false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Dentinogenesis imperfecta - Shield's type I Is a False Dentinogenesis imperfecta Inferred relationship Existential restriction modifier
    Dentinogenesis imperfecta - Shield's type II Is a False Dentinogenesis imperfecta Inferred relationship Existential restriction modifier
    Dentinogenesis imperfecta - Shield's type III Is a False Dentinogenesis imperfecta Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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