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60518002: Autosomal dominant epidermolysis bullosa simplex (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    100548013 Autosomal dominant epidermolysis bullosa simplex en Synonym Active Entire term case insensitive SNOMED CT core module
    100549017 EBS 1 en Synonym Active Entire term case sensitive SNOMED CT core module
    100550017 Epidermolysis bullosa simplex, Ogna type en Synonym Active Only initial character case insensitive SNOMED CT core module
    498765016 Epidermolysis bullosa simplex of Ogna en Synonym Active Only initial character case insensitive SNOMED CT core module
    799479010 Autosomal dominant epidermolysis bullosa simplex (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
    Autosomal dominant epidermolysis bullosa simplex Is a Epidermolysis bullosa simplex false Inferred relationship Existential restriction modifier
    Autosomal dominant epidermolysis bullosa simplex Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier
    Autosomal dominant epidermolysis bullosa simplex Associated morphology Blister false Inferred relationship Existential restriction modifier 2
    Autosomal dominant epidermolysis bullosa simplex Associated morphology Epidermolysis false Inferred relationship Existential restriction modifier 2
    Autosomal dominant epidermolysis bullosa simplex Associated morphology Keratolysis false Inferred relationship Existential restriction modifier 2
    Autosomal dominant epidermolysis bullosa simplex Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Autosomal dominant epidermolysis bullosa simplex Finding site Connective tissue false Inferred relationship Existential restriction modifier
    Autosomal dominant epidermolysis bullosa simplex Occurrence Congenital false Inferred relationship Existential restriction modifier
    Autosomal dominant epidermolysis bullosa simplex Finding site Structure of musculoskeletal system false Inferred relationship Existential restriction modifier
    Autosomal dominant epidermolysis bullosa simplex Finding site Connective tissue structure false Inferred relationship Existential restriction modifier
    Autosomal dominant epidermolysis bullosa simplex Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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