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4170004: Ehlers-Danlos syndrome, procollagen proteinase resistant (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
    8443014 Ehlers-Danlos syndrome, procollagen proteinase resistant en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    8444015 Ehlers-Danlos syndrome, mutant procollagen type 7 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    8445019 Ehlers-Danlos syndrome, autosomal dominant type 7 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    778518012 Ehlers-Danlos syndrome, procollagen proteinase resistant (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    8443014 Ehlers-Danlos syndrome, procollagen proteinase resistant en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    8444015 Ehlers-Danlos syndrome, mutant procollagen type 7 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    8445019 Ehlers-Danlos syndrome, autosomal dominant type 7 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    778518012 Ehlers-Danlos syndrome, procollagen proteinase resistant (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    778518012 Ehlers-Danlos syndrome, procollagen proteinase resistant (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    4402051000241119 syndrome d'Ehlers-Danlos de type 7B fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    4402051000241119 syndrome d'Ehlers-Danlos de type 7B fr Synonym (core metadata concept) Active Only initial character case insensitive (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 de type 7B Is a Ehlers-Danlos syndrome false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome d'Ehlers-Danlos de type 7B Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome d'Ehlers-Danlos de type 7B Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos de type 7B Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos de type 7B Finding site Connective tissue false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome d'Ehlers-Danlos de type 7B Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos de type 7B Finding site Connective tissue structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos de type 7B Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos de type 7B Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos de type 7B Is a Ehlers-Danlos syndrome (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    syndrome d'Ehlers-Danlos de type 7B Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos de type 7B Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos de type 7B Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos de type 7B Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome d'Ehlers-Danlos de type 7B Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome d'Ehlers-Danlos de type 7B Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome d'Ehlers-Danlos de type 7B Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome d'Ehlers-Danlos de type 7B Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome d'Ehlers-Danlos de type 7B Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome d'Ehlers-Danlos de type 7B Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome d'Ehlers-Danlos de type 7B Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome d'Ehlers-Danlos de type 7B Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome d'Ehlers-Danlos de type 7B Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos de type 7B Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome d'Ehlers-Danlos de type 7B Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
    syndrome d'Ehlers-Danlos de type 7B Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
    syndrome d'Ehlers-Danlos de type 7B Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    syndrome d'Ehlers-Danlos de type 7B 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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