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402806000: Congenital/hereditary lentiginosis (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
    1781898014 Congenital/hereditary lentiginosis 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
    Congenital/hereditary lentiginosis (disorder) est un(e) (attribut) Lentiginosis (disorder) false Inferred relationship Some
    Congenital/hereditary lentiginosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
    Congenital/hereditary lentiginosis (disorder) est un(e) (attribut) Congenital disease false Inferred relationship Some
    Congenital/hereditary lentiginosis (disorder) morphologie associée (attribut) Structure showing abnormal deposition of pigment (morphologic abnormality) false Inferred relationship Some 1
    Congenital/hereditary lentiginosis (disorder) survenue (attribut) congénital false Inferred relationship Some
    Congenital/hereditary lentiginosis (disorder) morphologie associée (attribut) Increased melanin pigmentation false Inferred relationship Some 1
    Congenital/hereditary lentiginosis (disorder) morphologie associée (attribut) Increased melanin pigmentation false Inferred relationship Some 1
    Congenital/hereditary lentiginosis (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Hereditary lentiginosis (disorder) est un(e) (attribut) False Congenital/hereditary lentiginosis (disorder) Inferred relationship Some
    Nevoid lentiginosis (disorder) est un(e) (attribut) False Congenital/hereditary lentiginosis (disorder) Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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