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22932004: Chondrodysplasia punctata, Conradi-Hünermann type (disorder)


    Status: retired, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    38517016 Chondrodysplasia punctata, Conradi-Hünermann type en Synonym Active Initial character case insensitive SNOMED CT core
    38518014 Conradi-Hünermann syndrome en Synonym Active Initial character case insensitive SNOMED CT core
    38519018 Conradi's syndrome en Synonym Active Case sensitive SNOMED CT core
    38520012 Chondrodysplasia punctata, Conradi-Hunermann type en Synonym Active Initial character case insensitive SNOMED CT core
    38521011 Conradi-Hunermann syndrome en Synonym Active Case sensitive SNOMED CT core
    481474011 Chondrodysplasia punctata, X-linked dominant type en Synonym Active Initial character case insensitive SNOMED CT core
    481475012 Chondrodysplasia calcificans congenita en Synonym Active Case insensitive SNOMED CT core
    752396018 Chondrodysplasia punctata, Conradi-Hünermann type (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Chondrodysplasia punctata, Conradi-Hünermann type Associated morphology Congenital dysplasia false Inferred relationship Some 2
    Chondrodysplasia punctata, Conradi-Hünermann type Is a Chondrodysplasia punctata false Inferred relationship Some
    Chondrodysplasia punctata, Conradi-Hünermann type Is a Cutaneous syndrome with ichthyosis false Inferred relationship Some
    Chondrodysplasia punctata, Conradi-Hünermann type Is a Hereditary disorder of musculoskeletal system false Inferred relationship Some
    Chondrodysplasia punctata, Conradi-Hünermann type Occurrence Congenital false Inferred relationship Some
    Chondrodysplasia punctata, Conradi-Hünermann type Finding site Bone structure false Inferred relationship Some 2
    Chondrodysplasia punctata, Conradi-Hünermann type Finding site Structure of skin region false Inferred relationship Some
    Chondrodysplasia punctata, Conradi-Hünermann type Associated morphology Dysplasia false Inferred relationship Some 1
    Chondrodysplasia punctata, Conradi-Hünermann type Finding site Skeletal system structure false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

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