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86667008: Ehlers-Danlos syndrome, dominant type 4 (disorder)

    Status: retired, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    143735010 Ehlers-Danlos syndrome, dominant type 4 en Synonym Active Case sensitive SNOMED CT core
    828978014 Ehlers-Danlos syndrome, dominant type 4 (disorder) en Fully specified name Active Case sensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

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

    Reference Sets

    Concept inactivation indicator reference set

    Description inactivation indicator reference set

    REPLACED BY association reference set

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