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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
    837491000052112 Ehlers-Danlos syndrom, recessiv typ 4 sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Ehlers-Danlos syndrom, recessiv typ 4 Is a Ehlers-Danlos syndrome, hydroxylysine-deficient false Inferred relationship Some
    Ehlers-Danlos syndrom, recessiv typ 4 Is a Vascular Ehlers-Danlos syndrome false Inferred relationship Some
    Ehlers-Danlos syndrom, recessiv typ 4 Associated morphology Dysplasia false Inferred relationship Some 1
    Ehlers-Danlos syndrom, recessiv typ 4 Finding site Skeletal system structure false Inferred relationship Some 1
    Ehlers-Danlos syndrom, recessiv typ 4 Occurrence Congenital false Inferred relationship Some
    Ehlers-Danlos syndrom, recessiv typ 4 Finding site Bone structure false Inferred relationship Some 1
    Ehlers-Danlos syndrom, recessiv typ 4 Finding site Skin structure false Inferred relationship Some 1
    Ehlers-Danlos syndrom, recessiv typ 4 Finding site Connective tissue false Inferred relationship Some
    Ehlers-Danlos syndrom, recessiv typ 4 Finding site Connective tissue structure false Inferred relationship Some 1
    Ehlers-Danlos syndrom, recessiv typ 4 Associated morphology kongenital dysplasi false Inferred relationship Some 1
    Ehlers-Danlos syndrom, recessiv typ 4 Finding site Bone structure false Inferred relationship Some 1
    Ehlers-Danlos syndrom, recessiv typ 4 Associated morphology kongenital dysplasi false Inferred relationship Some 1
    Ehlers-Danlos syndrom, recessiv typ 4 Finding site Skin structure false Inferred relationship Some 1
    Ehlers-Danlos syndrom, recessiv typ 4 Occurrence Congenital false Inferred relationship Some 2
    Ehlers-Danlos syndrom, recessiv typ 4 Associated morphology kongenital dysplasi false Inferred relationship Some 2
    Ehlers-Danlos syndrom, recessiv typ 4 Finding site Bone structure false Inferred relationship Some 2
    Ehlers-Danlos syndrom, recessiv typ 4 Occurrence Congenital false Inferred relationship Some 3
    Ehlers-Danlos syndrom, recessiv typ 4 Associated morphology kongenital dysplasi false Inferred relationship Some 3
    Ehlers-Danlos syndrom, recessiv typ 4 Finding site Skin structure false Inferred relationship Some 3
    Ehlers-Danlos syndrom, recessiv typ 4 Finding site Skin structure false Inferred relationship Some 2
    Ehlers-Danlos syndrom, recessiv typ 4 Finding site Bone structure false Inferred relationship Some 3
    Ehlers-Danlos syndrom, recessiv typ 4 Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Ehlers-Danlos syndrom, recessiv typ 4 Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
    Ehlers-Danlos syndrom, recessiv typ 4 Pathological process (attribute) Pathological developmental process false Inferred relationship Some 3
    Ehlers-Danlos syndrom, recessiv typ 4 Associated morphology Dysplasia false Inferred relationship Some 2
    Ehlers-Danlos syndrom, recessiv typ 4 Associated morphology Dysplasia false Inferred relationship Some 3
    Ehlers-Danlos syndrom, recessiv typ 4 Occurrence Congenital false Inferred relationship Some 1
    Ehlers-Danlos syndrom, recessiv typ 4 Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 1
    Ehlers-Danlos syndrom, recessiv typ 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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