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403791000: Keratoderma with deafness (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
    1782801014 Keratoderma with deafness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1771717015 Keratoderma with deafness (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1771717015 Keratoderma with deafness (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1782801014 Keratoderma with deafness en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1782801014 Keratoderma with deafness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) 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 Existential restriction modifier (core metadata concept)
    Keratoderma with deafness Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Keratoderma with deafness Has definitional manifestation Abnormal keratinization false Inferred relationship Existential restriction modifier (core metadata concept)
    Keratoderma with deafness Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Keratoderma with deafness Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Keratoderma with deafness Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Keratoderma with deafness Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Keratoderma with deafness Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Keratoderma with deafness Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Keratoderma with deafness Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Keratoderma with deafness Associated morphology Hyperkeratosis false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

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