FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

416633008: congenitale hereditaire endotheeldystrofie type 1 (aandoening)


    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
    6573541000146114 congenitale hereditaire endotheeldystrofie type 1 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    6573551000146112 congenitale hereditaire endotheeldystrofie type 1 (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    congenitale hereditaire endotheeldystrofie type 1 Is a Congenital hereditary endothelial dystrophy (disorder) false Inferred relationship Some
    congenitale hereditaire endotheeldystrofie type 1 Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 1
    congenitale hereditaire endotheeldystrofie type 1 Finding site Corneal structure false Inferred relationship Some 1
    congenitale hereditaire endotheeldystrofie type 1 Finding site Chromosome pair 20 false Inferred relationship Some 1
    congenitale hereditaire endotheeldystrofie type 1 Occurrence Congenital false Inferred relationship Some
    congenitale hereditaire endotheeldystrofie type 1 Associated morphology Dystrophy false Inferred relationship Some 1
    congenitale hereditaire endotheeldystrofie type 1 Associated morphology Dystrophy false Inferred relationship Some 2
    congenitale hereditaire endotheeldystrofie type 1 Finding site Structure of corneal endothelium false Inferred relationship Some 2
    congenitale hereditaire endotheeldystrofie type 1 Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some
    congenitale hereditaire endotheeldystrofie type 1 Associated morphology Dystrophy false Inferred relationship Some 1
    congenitale hereditaire endotheeldystrofie type 1 Finding site Structure of corneal endothelium false Inferred relationship Some 1
    congenitale hereditaire endotheeldystrofie type 1 Occurrence Congenital false Inferred relationship Some 2
    congenitale hereditaire endotheeldystrofie type 1 Finding site Chromosome pair 20 false Inferred relationship Some 2
    congenitale hereditaire endotheeldystrofie type 1 Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Some 2
    congenitale hereditaire endotheeldystrofie type 1 Is a Autosomal dominant hereditary disorder false Inferred relationship Some
    congenitale hereditaire endotheeldystrofie type 1 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)

    Back to Start