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72687002: Congenital pseudoarthrosis (morphologic abnormality)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Feb 2024. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    120743012 Congenital pseudoarthrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    812991017 Congenital pseudoarthrosis (morphologic abnormality) 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
    Congenital pseudoarthrosis Is a Congenital abnormal fusion false Inferred relationship Some
    Congenital pseudoarthrosis Is a Pseudoarthrosis false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Congenital pseudoarthrosis of tibia (disorder) Associated morphology False Congenital pseudoarthrosis Inferred relationship Some 1
    Congenital pseudoarthrosis of clavicle (disorder) Associated morphology False Congenital pseudoarthrosis Inferred relationship Some 1
    Congenital pseudoarthrosis of tibia (disorder) Associated morphology False Congenital pseudoarthrosis Inferred relationship Some 1
    Congenital pseudoarthrosis of clavicle (disorder) Associated morphology False Congenital pseudoarthrosis Inferred relationship Some 4
    Congenital pseudoarthrosis of tibia (disorder) Associated morphology False Congenital pseudoarthrosis Inferred relationship Some 3
    A rare, genetic, non-syndromic limb malformation characterized by delayed union or non-union of a long bone, resulting in formation of a false joint, with abnormal mobility and angulation at the pseudoarthrosis site, which manifests with progressive anterolateral forearm or leg bowing, limb shortening, and non-healing fractures. Typical histopathological findings include fibromatosis-like proliferation in the soft tissues with cystic or dysplastic lesions. Neurofibromatosis and osteofibrous dysplasia are frequently associated. Associated morphology False Congenital pseudoarthrosis Inferred relationship Some 1

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    US English

    REPLACED BY association reference set (foundation metadata concept)

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