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416633008: Congenital hereditary endothelial dystrophy type 1 (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2024. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    3644846012 Congenital hereditary endothelial dystrophy type 1 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3644847015 Congenital hereditary endothelial dystrophy autosomal dominant form en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3644848013 Congenital hereditary endothelial dystrophy type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3644852013 CHED1 - congenital hereditary endothelial dystrophy type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    927891000172114 CHED (congenital hereditary endothelial dystrophy) autosomique dominante fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    944291000172116 dystrophie endothéliale congénitale héréditaire type I fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    612361000274112 CHED1 - Kongenitale hereditäre Endotheldystrophie, Typ 1 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    612371000274116 Kongenitale hereditäre Endotheldystrophie, Typ 1 de 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
    dystrophie endothéliale congénitale héréditaire type I Is a Congenital hereditary endothelial dystrophy (disorder) false Inferred relationship Some
    dystrophie endothéliale congénitale héréditaire type I Associated morphology anomalie congénitale false Inferred relationship Some 1
    dystrophie endothéliale congénitale héréditaire type I Finding site Corneal structure false Inferred relationship Some 1
    dystrophie endothéliale congénitale héréditaire type I Finding site Chromosome pair 20 false Inferred relationship Some 1
    dystrophie endothéliale congénitale héréditaire type I Occurrence Congenital false Inferred relationship Some
    dystrophie endothéliale congénitale héréditaire type I Associated morphology Dystrophy false Inferred relationship Some 1
    dystrophie endothéliale congénitale héréditaire type I Associated morphology Dystrophy false Inferred relationship Some 2
    dystrophie endothéliale congénitale héréditaire type I Finding site Structure of corneal endothelium false Inferred relationship Some 2
    dystrophie endothéliale congénitale héréditaire type I Associated morphology anomalie congénitale false Inferred relationship Some
    dystrophie endothéliale congénitale héréditaire type I Associated morphology Dystrophy false Inferred relationship Some 1
    dystrophie endothéliale congénitale héréditaire type I Finding site Structure of corneal endothelium false Inferred relationship Some 1
    dystrophie endothéliale congénitale héréditaire type I Occurrence Congenital false Inferred relationship Some 2
    dystrophie endothéliale congénitale héréditaire type I Finding site Chromosome pair 20 false Inferred relationship Some 2
    dystrophie endothéliale congénitale héréditaire type I Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Some 2
    dystrophie endothéliale congénitale héréditaire type I Is a Autosomal dominant hereditary disorder (disorder) false Inferred relationship Some
    dystrophie endothéliale congénitale héréditaire type I Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2

    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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