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402741006: Skin damage resulting from congenital/hereditary neuropathy (disorder)

    Status: retired, Primitive. Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    1770665016 Skin damage resulting from congenital/hereditary neuropathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
    1781838011 Skin damage resulting from congenital/hereditary neuropathy en Synonym Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Skin damage resulting from congenital/hereditary neuropathy Due to Peripheral neuropathy false Inferred relationship Some 1
    Skin damage resulting from congenital/hereditary neuropathy Is a Dermatosis due to peripheral nerve disorder false Inferred relationship Some
    Skin damage resulting from congenital/hereditary neuropathy Finding site Skin structure false Inferred relationship Some 2
    Skin damage resulting from congenital/hereditary neuropathy Is a Congenital disease false Inferred relationship Some
    Skin damage resulting from congenital/hereditary neuropathy Occurrence Congenital false Inferred relationship Some
    Skin damage resulting from congenital/hereditary neuropathy Associated with Peripheral neuropathy false Inferred relationship Some
    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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