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86781004: Hemochromatosis (disorder)


    Status: retired, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    143918018 Hemochromatosis en Synonym Active Case insensitive SNOMED CT core
    143921016 Bronzed cirrhosis en Synonym Active Case insensitive SNOMED CT core
    143922011 Pigmentary cirrhosis of liver en Synonym Active Case insensitive SNOMED CT core
    143923018 von Recklinghausen-Appelbaum disease en Synonym Active Case sensitive SNOMED CT core
    143924012 Iron storage disease en Synonym Active Case insensitive SNOMED CT core
    507253013 Familial hemochromatosis en Synonym Active Case insensitive SNOMED CT core
    507254019 Hereditary hemochromatosis en Synonym Active Case insensitive SNOMED CT core
    507255018 Primary hemochromatosis en Synonym Active Case insensitive SNOMED CT core
    507256017 Idiopathic hemochromatosis en Synonym Active Case insensitive SNOMED CT core
    507257014 Familial haemochromatosis en Synonym Active Case insensitive SNOMED CT core
    507258016 Hereditary haemochromatosis en Synonym Active Case insensitive SNOMED CT core
    507259012 Idiopathic haemochromatosis en Synonym Active Case insensitive SNOMED CT core
    507260019 Primary haemochromatosis en Synonym Active Case insensitive SNOMED CT core
    507261015 Bronzed diabetes en Synonym Active Case insensitive SNOMED CT core
    507262010 von Recklinghausen-Applebaum disease en Synonym Active Case sensitive SNOMED CT core
    507263017 Haemochromatosis en Synonym Active Case insensitive SNOMED CT core
    829117016 Hemochromatosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Haemochromatosis Is a Iron overload false Inferred relationship Some
    Haemochromatosis Is a Metabolic and genetic disorder affecting the liver false Inferred relationship Some
    Haemochromatosis Finding site Liver structure false Inferred relationship Some
    Haemochromatosis Causative agent Iron false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Hereditary haemochromatosis Is a False Haemochromatosis Inferred relationship Some
    Juvenile haemochromatosis Is a False Haemochromatosis Inferred relationship Some
    Secondary haemochromatosis Is a False Haemochromatosis Inferred relationship Some
    Restrictive cardiomyopathy secondary to haemochromatosis Is a False Haemochromatosis Inferred relationship Some
    Neonatal haemochromatosis Is a False Haemochromatosis Inferred relationship Some
    Dilated cardiomyopathy due to haemochromatosis Is a False Haemochromatosis Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

    SAME AS association reference set

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