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402806000: Congenital/hereditary lentiginosis (disorder)

    Status: retired, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    1770730013 Congenital/hereditary lentiginosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
    1781898014 Congenital/hereditary lentiginosis en Synonym Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital/hereditary lentiginosis Is a Lentiginosis false Inferred relationship Some
    Congenital/hereditary lentiginosis Finding site Skin structure false Inferred relationship Some 1
    Congenital/hereditary lentiginosis Is a Congenital disease false Inferred relationship Some
    Congenital/hereditary lentiginosis Associated morphology Pigment deposition false Inferred relationship Some 1
    Congenital/hereditary lentiginosis Occurrence Congenital false Inferred relationship Some
    Congenital/hereditary lentiginosis Associated morphology Increased melanin pigmentation false Inferred relationship Some 1
    Congenital/hereditary lentiginosis Associated morphology Increased melanin pigmentation false Inferred relationship Some 1
    Congenital/hereditary lentiginosis Finding site Skin structure false Inferred relationship Some 1
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Hereditary lentiginosis Is a False Congenital/hereditary lentiginosis Inferred relationship Some
    Naevoid lentiginosis Is a False Congenital/hereditary lentiginosis Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

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