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7096005: Meningomyelocele (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2005. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    12704019 Meningomyelocele en Synonym Active Entire term case insensitive SNOMED CT core module
    12709012 Myelocystocele en Synonym Active Entire term case insensitive SNOMED CT core module
    12710019 Myelomeningocele en Synonym Active Entire term case insensitive SNOMED CT core module
    501729014 Thoracic spinal hydromeningocele en Synonym Active Entire term case insensitive SNOMED CT core module
    811073014 Meningomyelocele (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Meningomyelocele Is a Congenital anomaly of spinal meninges false Inferred relationship Existential restriction modifier
    Meningomyelocele Is a Disorder of thorax false Inferred relationship Existential restriction modifier
    Meningomyelocele Is a Meningomyelocele/myelocele false Inferred relationship Existential restriction modifier
    Meningomyelocele Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
    Meningomyelocele Associated morphology Congenital protrusion false Inferred relationship Existential restriction modifier
    Meningomyelocele Finding site Spinal cord meninges structure false Inferred relationship Existential restriction modifier 1
    Meningomyelocele Finding site Spinal cord structure false Inferred relationship Existential restriction modifier 2
    Meningomyelocele Occurrence Congenital false Inferred relationship Existential restriction modifier
    Meningomyelocele Associated morphology Congenital failure of fusion false Inferred relationship Existential restriction modifier
    Meningomyelocele Finding site Bone structure of spine false Inferred relationship Existential restriction modifier 2
    Meningomyelocele Is a Myelocele false Inferred relationship Existential restriction modifier
    Meningomyelocele Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Meningomyelocele Associated morphology Congenital failure of fusion with herniated tissue false Inferred relationship Existential restriction modifier 2
    Meningomyelocele Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier 2
    Meningomyelocele Associated morphology Protrusion false Inferred relationship Existential restriction modifier
    Meningomyelocele Is a Congenital anomaly of spine false Inferred relationship Existential restriction modifier
    Meningomyelocele Is a Congenital malformation false Inferred relationship Existential restriction modifier
    Meningomyelocele Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 3
    Meningomyelocele Finding site Structure of nervous system false Inferred relationship Existential restriction modifier 3
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Known OR suspected fetal spina bifida with myelomeningocele affecting obstetrical care Is a False Meningomyelocele Inferred relationship Existential restriction modifier
    Fetal myelomeningocele causing disproportion Is a False Meningomyelocele Inferred relationship Existential restriction modifier
    Meningomyelocele/myelocele Is a False Meningomyelocele Inferred relationship Existential restriction modifier
    Hydromeningomyelocele Is a False Meningomyelocele Inferred relationship Existential restriction modifier
    Hydromeningomyelocele Is a False Meningomyelocele Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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