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205490002: Osteodysplasia (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    315109012 Osteodysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    590864016 Osteodysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Osteodysplasia survenue (attribut) congénital false Inferred relationship Some 1
    Osteodysplasia Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Osteodysplasia morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 1
    Osteodysplasia localisation d'une constatation (attribut) structure osseuse false Inferred relationship Some 1
    Osteodysplasia est un(e) (attribut) Skeletal dysplasia false Inferred relationship Some
    Osteodysplasia morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 1
    Osteodysplasia survenue (attribut) congénital false Inferred relationship Some 2
    Osteodysplasia localisation d'une constatation (attribut) structure osseuse false Inferred relationship Some 2
    Osteodysplasia morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 2
    Osteodysplasia localisation d'une constatation (attribut) structure osseuse false Inferred relationship Some 1
    Osteodysplasia morphologie associée (attribut) dysplasie false Inferred relationship Some 1
    Osteodysplasia localisation d'une constatation (attribut) Skeletal system structure false Inferred relationship Some 1
    Osteodysplasia survenue (attribut) congénital false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Familial osteodysplasia Anderson type (disorder) est un(e) (attribut) False Osteodysplasia Inferred relationship Some
    Osteochondrodysplasia est un(e) (attribut) False Osteodysplasia Inferred relationship Some
    Osteodysplasia, unspecified est un(e) (attribut) False Osteodysplasia Inferred relationship Some
    Other osteodysplasia NOS est un(e) (attribut) False Osteodysplasia Inferred relationship Some
    Other specified osteodysplasia est un(e) (attribut) False Osteodysplasia Inferred relationship Some
    Osteodysplasia NOS est un(e) (attribut) False Osteodysplasia Inferred relationship Some
    Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (disorder) est un(e) (attribut) False Osteodysplasia Inferred relationship Some
    syndrome oto-palato-digital type 2 (trouble) est un(e) (attribut) False Osteodysplasia Inferred relationship Some
    syndrome oto-palato-digital type 1 (trouble) est un(e) (attribut) False Osteodysplasia Inferred relationship Some
    Otopalatodigital syndrome est un(e) (attribut) False Osteodysplasia Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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