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236420000: Alport syndrome-like hereditary nephritis (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
    354402019 Alport syndrome-like hereditary nephritis en Synonym Active Entire term case sensitive SNOMED CT core module
    625010010 Alport syndrome-like hereditary nephritis (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Alport syndrome-like hereditary nephritis Is a Hereditary nephritis false Inferred relationship Existential restriction modifier
    Alport syndrome-like hereditary nephritis Finding site Kidney structure false Inferred relationship Existential restriction modifier 1
    Alport syndrome-like hereditary nephritis Associated morphology Basement membrane alteration false Inferred relationship Existential restriction modifier
    Alport syndrome-like hereditary nephritis Course Chronic false Inferred relationship Existential restriction modifier
    Alport syndrome-like hereditary nephritis Associated morphology Chronic inflammation false Inferred relationship Existential restriction modifier 1
    Alport syndrome-like hereditary nephritis Finding site Glomerulus structure false Inferred relationship Existential restriction modifier 1
    Alport syndrome-like hereditary nephritis Has definitional manifestation Blood in urine false Inferred relationship Existential restriction modifier
    Alport syndrome-like hereditary nephritis Is a Hereditary nephritis false Inferred relationship Existential restriction modifier
    Alport syndrome-like hereditary nephritis Course Chronic false Inferred relationship Existential restriction modifier
    Alport syndrome-like hereditary nephritis Associated morphology Chronic inflammation false Inferred relationship Existential restriction modifier 1
    Alport syndrome-like hereditary nephritis Finding site Glomerulus structure false Inferred relationship Existential restriction modifier 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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