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191240007: Erythrogenesis imperfecta (disorder)

    Status: retired, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    294178016 Erythrogenesis imperfecta en Synonym Active Case insensitive SNOMED CT core
    574917019 Erythrogenesis imperfecta (disorder) en Fully specified name Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Erythrogenesis imperfecta Is a Anaemia due to intrinsic red cell abnormality false Inferred relationship Some
    Erythrogenesis imperfecta Finding site Haematopoietic system structure false Inferred relationship Some
    Erythrogenesis imperfecta Has definitional manifestation Erythropenia false Inferred relationship Some
    Erythrogenesis imperfecta Is a Anaemia false Inferred relationship Some
    Erythrogenesis imperfecta Has interpretation Below reference range false Inferred relationship Some 1
    Erythrogenesis imperfecta Interprets Measurement of total haemoglobin concentration false Inferred relationship Some 1
    Erythrogenesis imperfecta Has interpretation Below reference range false Inferred relationship Some 2
    Erythrogenesis imperfecta Interprets Red blood cell count false Inferred relationship Some 2
    Erythrogenesis imperfecta Finding site Haematopoietic system structure false Inferred relationship Some
    Erythrogenesis imperfecta Finding site Erythrocyte false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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