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70610001: Ehlers-Danlos syndrome, recessive type 4 (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    117291014 Ehlers-Danlos syndrome, recessive type 4 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    810684011 Ehlers-Danlos syndrome, recessive type 4 (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Ehlers-Danlos syndrome, recessive type 4 Is a Ehlers-Danlos syndrome, hydroxylysine-deficient false Inferred relationship Some
    Ehlers-Danlos syndrome, recessive type 4 Is a Vascular Ehlers-Danlos syndrome false Inferred relationship Some
    Ehlers-Danlos syndrome, recessive type 4 Associated morphology Dysplasia false Inferred relationship Some 1
    Ehlers-Danlos syndrome, recessive type 4 Finding site Skeletal system structure false Inferred relationship Some 1
    Ehlers-Danlos syndrome, recessive type 4 Occurrence Congenital false Inferred relationship Some
    Ehlers-Danlos syndrome, recessive type 4 Finding site Bone structure false Inferred relationship Some 1
    Ehlers-Danlos syndrome, recessive type 4 Finding site Skin structure false Inferred relationship Some 1
    Ehlers-Danlos syndrome, recessive type 4 Finding site Connective tissue false Inferred relationship Some
    Ehlers-Danlos syndrome, recessive type 4 Finding site Connective tissue structure false Inferred relationship Some 1
    Ehlers-Danlos syndrome, recessive type 4 Associated morphology Congenital dysplasia false Inferred relationship Some 1
    Ehlers-Danlos syndrome, recessive type 4 Finding site Bone structure false Inferred relationship Some 1
    Ehlers-Danlos syndrome, recessive type 4 Associated morphology Congenital dysplasia false Inferred relationship Some 1
    Ehlers-Danlos syndrome, recessive type 4 Finding site Skin structure false Inferred relationship Some 1
    Ehlers-Danlos syndrome, recessive type 4 Occurrence Congenital false Inferred relationship Some 2
    Ehlers-Danlos syndrome, recessive type 4 Associated morphology Congenital dysplasia false Inferred relationship Some 2
    Ehlers-Danlos syndrome, recessive type 4 Finding site Bone structure false Inferred relationship Some 2
    Ehlers-Danlos syndrome, recessive type 4 Occurrence Congenital false Inferred relationship Some 3
    Ehlers-Danlos syndrome, recessive type 4 Associated morphology Congenital dysplasia false Inferred relationship Some 3
    Ehlers-Danlos syndrome, recessive type 4 Finding site Skin structure false Inferred relationship Some 3
    Ehlers-Danlos syndrome, recessive type 4 Finding site Skin structure false Inferred relationship Some 2
    Ehlers-Danlos syndrome, recessive type 4 Finding site Bone structure false Inferred relationship Some 3
    Ehlers-Danlos syndrome, recessive type 4 Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Ehlers-Danlos syndrome, recessive type 4 Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
    Ehlers-Danlos syndrome, recessive type 4 Pathological process (attribute) Pathological developmental process false Inferred relationship Some 3
    Ehlers-Danlos syndrome, recessive type 4 Associated morphology Dysplasia false Inferred relationship Some 2
    Ehlers-Danlos syndrome, recessive type 4 Associated morphology Dysplasia false Inferred relationship Some 3
    Ehlers-Danlos syndrome, recessive type 4 Occurrence Congenital false Inferred relationship Some 1
    Ehlers-Danlos syndrome, recessive type 4 Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 1
    Ehlers-Danlos syndrome, recessive type 4 Is a Autosomal recessive hereditary disorder false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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