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84852005: Multiple exostoses syndrome (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2004. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    140678013 Multiple exostoses syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    140679017 Diaphyseal aclasis, external chondromatosis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    506254014 Diaphyseal aclasis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    506255010 Osteochondromatosis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    506256011 Multiple cartilaginous exostoses en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    506257019 Hereditary deforming chondrodysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    826783019 Multiple exostoses syndrome (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
    Multiple exostoses syndrome Is a Disorganized development of cartilaginous and fibrous components of the skeleton false Inferred relationship Some
    Multiple exostoses syndrome Associated morphology Dysplasia false Inferred relationship Some 1
    Multiple exostoses syndrome Finding site Skeletal system structure false Inferred relationship Some 1
    Multiple exostoses syndrome Occurrence Congenital false Inferred relationship Some
    Multiple exostoses syndrome Finding site Bone structure false Inferred relationship Some 1
    Multiple exostoses syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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