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24353001: Meromicrosomia (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    40853012 Meromicrosomia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    753980018 Meromicrosomia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    69871000077112 microsomie partielle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    microsomie partielle Is a Longitudinal deficiency of limb false Inferred relationship Some
    microsomie partielle Occurrence Congenital false Inferred relationship Some
    microsomie partielle Associated morphology Abnormally short growth false Inferred relationship Some 1
    microsomie partielle Finding site Musculoskeletal structure of limb false Inferred relationship Some
    microsomie partielle Finding site Limb structure false Inferred relationship Some 1
    microsomie partielle Associated morphology anomalie du développement false Inferred relationship Some
    microsomie partielle Is a Congenital anomaly of musculoskeletal system false Inferred relationship Some
    microsomie partielle Finding site Structure of musculoskeletal system (body structure) false Inferred relationship Some 2
    microsomie partielle Associated morphology anomalie congénitale false Inferred relationship Some 2
    microsomie partielle Associated morphology Abnormally short growth false Inferred relationship Some 1
    microsomie partielle Finding site Limb structure false Inferred relationship Some 1
    microsomie partielle Finding site Structure of musculoskeletal system (body structure) false Inferred relationship Some 2
    microsomie partielle Associated morphology anomalie congénitale false Inferred relationship Some 2
    microsomie partielle Finding site Limb structure false Inferred relationship Some 1
    microsomie partielle Associated morphology anomalie congénitale false Inferred relationship Some 1
    microsomie partielle Occurrence Congenital false Inferred relationship Some 3
    microsomie partielle Associated morphology anomalie du développement false Inferred relationship Some 3
    microsomie partielle Finding site Structure of musculoskeletal system (body structure) false Inferred relationship Some 3
    microsomie partielle Occurrence Congenital false Inferred relationship Some 4
    microsomie partielle Finding site Limb structure false Inferred relationship Some 4
    microsomie partielle Associated morphology Abnormally short growth false Inferred relationship Some 4
    microsomie partielle Occurrence Congenital false Inferred relationship Some 2
    microsomie partielle Occurrence Congenital false Inferred relationship Some 1
    microsomie partielle Associated morphology Abnormal shortening false Inferred relationship Some 1
    microsomie partielle Finding site Limb structure false Inferred relationship Some 1
    microsomie partielle Associated morphology Abnormal shortening false Inferred relationship Some 2
    microsomie partielle Finding site Entire limb false Inferred relationship Some 2
    microsomie partielle Finding site Structure of musculoskeletal system (body structure) false Inferred relationship Some 1
    microsomie partielle Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 1
    microsomie partielle Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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