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254240003: Neurofibromatosis type 3 (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    378470019 Neurofibromatosis type 3 en Synonym Active Entire term case insensitive SNOMED CT core module
    645104019 Neurofibromatosis type 3 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    3009825010 Neurofibromatosis, type 3 en Synonym Active Entire term case insensitive SNOMED CT core module
    3011600012 NF 3 en Synonym Active Entire term case sensitive SNOMED CT core module
    3011959018 Mixed central and peripheral neurofibromatosis en Synonym Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Neurofibromatosis type 3 Is a Neurofibromatosis syndrome false Inferred relationship Existential restriction modifier
    Neurofibromatosis type 3 Occurrence Congenital false Inferred relationship Existential restriction modifier
    Neurofibromatosis type 3 Finding site Structure of nervous system false Inferred relationship Existential restriction modifier 1
    Neurofibromatosis type 3 Associated morphology Dysplasia false Inferred relationship Existential restriction modifier 2
    Neurofibromatosis type 3 Pathological process Neoplastic process false Inferred relationship Existential restriction modifier
    Neurofibromatosis type 3 Associated morphology Neurofibromatosis false Inferred relationship Existential restriction modifier 2
    Neurofibromatosis type 3 Finding site Structure of skin region false Inferred relationship Existential restriction modifier 2
    Neurofibromatosis type 3 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 3
    Neurofibromatosis type 3 Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Neurofibromatosis type 3 Associated morphology Hamartoma false Inferred relationship Existential restriction modifier
    Neurofibromatosis type 3 Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Neurofibromatosis type 3 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
    Neurofibromatosis type 3 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Neurofibromatosis type 3 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 3
    Neurofibromatosis type 3 Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Neurofibromatosis type 3 Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Neurofibromatosis type 3 Associated morphology Neoplasm false Inferred relationship Existential restriction modifier
    Neurofibromatosis type 3 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Neurofibromatosis type 3 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
    Neurofibromatosis type 3 Finding site Structure of nervous system false Inferred relationship Existential restriction modifier 1
    Neurofibromatosis type 3 Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Neurofibromatosis type 3 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Neurofibromatosis type 3 Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Neurofibromatosis type 3 Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
    Neurofibromatosis type 3 Finding site Structure of nervous system false Inferred relationship Existential restriction modifier 2
    Neurofibromatosis type 3 Occurrence Congenital false Inferred relationship Existential restriction modifier 3
    Neurofibromatosis type 3 Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
    Neurofibromatosis type 3 Finding site Skin structure false Inferred relationship Existential restriction modifier 3
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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