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402806000: Congenital/hereditary lentiginosis (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

    Descriptions:

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


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital/hereditary lentiginosis Is a Lentiginosis false Inferred relationship Existential restriction modifier
    Congenital/hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Congenital/hereditary lentiginosis Is a Congenital disease false Inferred relationship Existential restriction modifier
    Congenital/hereditary lentiginosis Associated morphology Structure showing abnormal deposition of pigment false Inferred relationship Existential restriction modifier 1
    Congenital/hereditary lentiginosis Occurrence Congenital false Inferred relationship Existential restriction modifier
    Congenital/hereditary lentiginosis Associated morphology Increased melanin pigmentation false Inferred relationship Existential restriction modifier 1
    Congenital/hereditary lentiginosis Associated morphology Increased melanin pigmentation false Inferred relationship Existential restriction modifier 1
    Congenital/hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 1

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Hereditary lentiginosis Is a False Congenital/hereditary lentiginosis Inferred relationship Existential restriction modifier
    Nevoid lentiginosis Is a False Congenital/hereditary lentiginosis Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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