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60518002: Autosomal dominant epidermolysis bullosa simplex (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    100548013 Autosomal dominant epidermolysis bullosa simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    100549017 EBS 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    100550017 Epidermolysis bullosa simplex, Ogna type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    498765016 Epidermolysis bullosa simplex of Ogna en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    799479010 Autosomal dominant epidermolysis bullosa simplex (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    100548013 Autosomal dominant epidermolysis bullosa simplex en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    100548013 Autosomal dominant epidermolysis bullosa simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    100549017 EBS 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    100550017 Epidermolysis bullosa simplex, Ogna type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    498765016 Epidermolysis bullosa simplex of Ogna en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    799479010 Autosomal dominant epidermolysis bullosa simplex (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    799479010 Autosomal dominant epidermolysis bullosa simplex (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

    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 (core metadata concept)
    Autosomal dominant epidermolysis bullosa simplex Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    Autosomal dominant epidermolysis bullosa simplex Associated morphology Blister (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Autosomal dominant epidermolysis bullosa simplex Associated morphology Epidermolysis (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Autosomal dominant epidermolysis bullosa simplex Associated morphology Keratolysis false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Autosomal dominant epidermolysis bullosa simplex Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Autosomal dominant epidermolysis bullosa simplex Finding site Connective tissue false Inferred relationship Existential restriction modifier (core metadata concept)
    Autosomal dominant epidermolysis bullosa simplex Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Autosomal dominant epidermolysis bullosa simplex Finding site Structure of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
    Autosomal dominant epidermolysis bullosa simplex Finding site Connective tissue structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    Autosomal dominant epidermolysis bullosa simplex Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

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