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75523000: Congenital hamartosis (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    125435017 Hamartosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2671536013 Congenital hamartosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    816143015 Congenital hamartosis (disorder) en Fully specified name 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 hamartosis est un(e) (attribut) Congenital hamartoma (disorder) false Inferred relationship Some
    Congenital hamartosis morphologie associée (attribut) Hamartoma (morphologic abnormality) false Inferred relationship Some
    Congenital hamartosis est un(e) (attribut) Congenital disease false Inferred relationship Some
    Congenital hamartosis survenue (attribut) congénital false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Centrofacial lentiginosis syndrome est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Neurofibromatosis syndrome est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Neurocutaneous melanosis sequence est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    maladie de Rendu-Osler est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Riley-Smith syndrome est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Goltz syndrome est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Proteus syndrome est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Moynahan's syndrome est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Sturge-Weber syndrome (disorder) est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Ruvalcaba-Myhre syndrome est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    syndrome de Maffucci (trouble) est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    maladie de von Hippel-Lindau (trouble) est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Linear sebaceous naevus sequence est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    syndrome des hamartomes multiples (trouble) est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    angiodysplasie ostéodystrophique est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Gardner syndrome est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Turcot syndrome est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Cerebrofacial arteriovenous metameric syndrome type 2 est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Lhermitte-Duclos disease est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Vascular hamartoma of skin est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Tuberous sclerosis syndrome est un(e) (attribut) False Congenital hamartosis Inferred relationship Some
    Multiple lentigines syndrome est un(e) (attribut) False Congenital hamartosis Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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