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367511000119101: Hereditary mesangiocapillary glomerulonephritis, type 2 (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Oct 2021. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    3012571015 Hereditary mesangiocapillary glomerulonephritis, type 2 en Synonym Active Entire term case insensitive SNOMED CT core module
    3012580015 Hereditary mesangiocapillary glomerulonephritis, type 2 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    3289093011 Hereditary dense deposit disease 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
    Hereditary mesangiocapillary glomerulonephritis, type 2 Is a Hereditary diffuse mesangial proliferative glomerulonephritis false Inferred relationship Existential restriction modifier
    Hereditary mesangiocapillary glomerulonephritis, type 2 Clinical course Chronic false Inferred relationship Existential restriction modifier 1
    Hereditary mesangiocapillary glomerulonephritis, type 2 Associated morphology Chronic proliferative inflammation false Inferred relationship Existential restriction modifier 2
    Hereditary mesangiocapillary glomerulonephritis, type 2 Finding site Structure of glomerular mesangium false Inferred relationship Existential restriction modifier 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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