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83470009: Ehlers-Danlos syndrome, type 1 (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2023. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    138440018 Ehlers-Danlos syndrome, type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    138441019 Ehlers-Danlos syndrome, severe classic form en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    138442014 Ehlers-Danlos syndrome, gravis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    825110010 Ehlers-Danlos syndrome, type 1 (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    1234831013 Ehlers-Danlos syndrome type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    138440018 Ehlers-Danlos syndrome, type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    138441019 Ehlers-Danlos syndrome, severe classic form en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    138442014 Ehlers-Danlos syndrome, gravis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    825110010 Ehlers-Danlos syndrome, type 1 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    825110010 Ehlers-Danlos syndrome, type 1 (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    1234831013 Ehlers-Danlos syndrome type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1234831013 Ehlers-Danlos syndrome type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    884231000172119 EDS I - Ehlers-Danlos syndrome type 1 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    950051000172113 syndrome d'Ehlers-Danlos type 1 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    884231000172119 EDS I - Ehlers-Danlos syndrome type 1 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    950051000172113 syndrome d'Ehlers-Danlos type 1 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    syndrome d'Ehlers-Danlos type 1 Is a Ehlers-Danlos syndrome false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome d'Ehlers-Danlos type 1 Severity Severe false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome d'Ehlers-Danlos type 1 Finding site Connective tissue structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos type 1 Finding site Connective tissue false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome d'Ehlers-Danlos type 1 Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos type 1 Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos type 1 Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos type 1 Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome d'Ehlers-Danlos type 1 Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos type 1 Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos type 1 Is a Ehlers-Danlos syndrome (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome d'Ehlers-Danlos type 1 Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos type 1 Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos type 1 Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos type 1 Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome d'Ehlers-Danlos type 1 Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome d'Ehlers-Danlos type 1 Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome d'Ehlers-Danlos type 1 Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome d'Ehlers-Danlos type 1 Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome d'Ehlers-Danlos type 1 Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome d'Ehlers-Danlos type 1 Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome d'Ehlers-Danlos type 1 Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome d'Ehlers-Danlos type 1 Is a A rare inherited connective tissue disorder characterized by skin hyperextensibility, widened atrophic scars, and generalized joint hypermobility. false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome d'Ehlers-Danlos type 1 Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos type 1 Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome d'Ehlers-Danlos type 1 Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome d'Ehlers-Danlos type 1 Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome d'Ehlers-Danlos type 1 Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome d'Ehlers-Danlos type 1 Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos type 1 Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

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

    REPLACED BY association reference set (foundation metadata concept)

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