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254057007: Omodysplasia II (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    378203019 Omodysplasia II en Synonym Active Only initial character case insensitive SNOMED CT core module
    378204013 Omodysplasia, Borochowitz type en Synonym Active Only initial character case insensitive SNOMED CT core module
    644896018 Omodysplasia II (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Omodysplasia II Is a Atelosteogenesis false Inferred relationship Existential restriction modifier
    Omodysplasia II Finding site Bone structure false Inferred relationship Existential restriction modifier 1
    Omodysplasia II Occurrence Congenital false Inferred relationship Existential restriction modifier
    Omodysplasia II Finding site Skeletal system structure false Inferred relationship Existential restriction modifier 1
    Omodysplasia II Associated morphology Dysplasia false Inferred relationship Existential restriction modifier 1
    Omodysplasia II Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
    Omodysplasia II Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
    Omodysplasia II Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
    Omodysplasia II Finding site Bone structure false Inferred relationship Existential restriction modifier 1
    Omodysplasia II Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Omodysplasia II Finding site Bone structure false Inferred relationship Existential restriction modifier 2
    Omodysplasia II Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2

    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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