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75523000: Congenital hamartosis (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    125435017 Hamartosis en Synonym Active Entire term case insensitive SNOMED CT core module
    816143015 Congenital hamartosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    2671536013 Congenital hamartosis 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 hamartosis Is a Congenital disease false Inferred relationship Existential restriction modifier
    Congenital hamartosis Occurrence Congenital false Inferred relationship Existential restriction modifier
    Congenital hamartosis Is a Congenital hamartoma false Inferred relationship Existential restriction modifier
    Congenital hamartosis Associated morphology Hamartoma false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Multiple lentigines syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Centrofacial lentiginosis syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Neurofibromatosis syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Neurocutaneous melanosis sequence Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Osler hemorrhagic telangiectasia syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Riley-Smith syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Goltz syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Proteus syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Moynahan's syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Ruvalcaba-Myhre syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Maffucci syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Von Hippel-Lindau syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Linear sebaceous nevus sequence Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Cowden syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Klippel-Trenaunay-Weber syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Gardner syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Turcot syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Cerebral-retinal arteriovenous aneurysm Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Lhermitte-Duclos disease Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Vascular hamartoma of skin Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Tuberous sclerosis syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier
    Sturge-Weber syndrome Is a False Congenital hamartosis Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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