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403791000: Keratoderma with deafness (disorder)

    Status: retired, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    1771717015 Keratoderma with deafness (disorder) en Fully specified name Active Case insensitive SNOMED CT core
    1782801014 Keratoderma with deafness en Synonym Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Keratoderma with deafness Is a Hereditary palmoplantar keratoderma false Inferred relationship Some
    Keratoderma with deafness Occurrence Congenital false Inferred relationship Some
    Keratoderma with deafness Has definitional manifestation Abnormal keratinisation false Inferred relationship Some
    Keratoderma with deafness Finding site Skin structure false Inferred relationship Some 1
    Keratoderma with deafness Associated morphology Congenital anomaly false Inferred relationship Some 1
    Keratoderma with deafness Finding site Skin structure false Inferred relationship Some 1
    Keratoderma with deafness Associated morphology Congenital anomaly false Inferred relationship Some 1
    Keratoderma with deafness Occurrence Congenital false Inferred relationship Some 2
    Keratoderma with deafness Associated morphology Developmental abnormality false Inferred relationship Some 2
    Keratoderma with deafness Finding site Skin structure false Inferred relationship Some 2
    Keratoderma with deafness Associated morphology Hyperkeratosis 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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