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86781004: Hemochromatosis (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    143918018 Hemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
    143919014 Hemochromatosis, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
    143920015 Iron storage disease, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
    143921016 Bronzed cirrhosis en Synonym Active Entire term case insensitive SNOMED CT core module
    143922011 Pigmentary cirrhosis of liver en Synonym Active Entire term case insensitive SNOMED CT core module
    143923018 von Recklinghausen-Appelbaum disease en Synonym Active Entire term case sensitive SNOMED CT core module
    143924012 Iron storage disease en Synonym Active Entire term case insensitive SNOMED CT core module
    507253013 Familial hemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
    507254019 Hereditary hemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
    507255018 Primary hemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
    507256017 Idiopathic hemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
    507257014 Familial haemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
    507258016 Hereditary haemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
    507259012 Idiopathic haemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
    507260019 Primary haemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
    507261015 Bronzed diabetes en Synonym Active Entire term case insensitive SNOMED CT core module
    507262010 von Recklinghausen-Applebaum disease en Synonym Active Entire term case sensitive SNOMED CT core module
    507263017 Haemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
    829117016 Hemochromatosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Hemochromatosis Is a Iron overload false Inferred relationship Existential restriction modifier
    Hemochromatosis Is a Metabolic and genetic disorder affecting the liver false Inferred relationship Existential restriction modifier
    Hemochromatosis Finding site Liver structure false Inferred relationship Existential restriction modifier
    Hemochromatosis Causative agent Iron false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Hereditary hemochromatosis Is a False Hemochromatosis Inferred relationship Existential restriction modifier
    Juvenile hemochromatosis Is a False Hemochromatosis Inferred relationship Existential restriction modifier
    Secondary hemochromatosis Is a False Hemochromatosis Inferred relationship Existential restriction modifier
    Restrictive cardiomyopathy secondary to hemochromatosis Is a False Hemochromatosis Inferred relationship Existential restriction modifier
    Neonatal hemochromatosis Is a False Hemochromatosis Inferred relationship Existential restriction modifier
    Dilated cardiomyopathy due to hemochromatosis Is a False Hemochromatosis Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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