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86781004: Hemochromatosis (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    143918018 Hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    143921016 Bronzed cirrhosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    143922011 Pigmentary cirrhosis of liver en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    143923018 von Recklinghausen-Appelbaum disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    143924012 Iron storage disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507253013 Familial hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507254019 Hereditary hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507255018 Primary hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507256017 Idiopathic hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507257014 Familial haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507258016 Hereditary haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507259012 Idiopathic haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507260019 Primary haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507261015 Bronzed diabetes en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507262010 von Recklinghausen-Applebaum disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    507263017 Haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    829117016 Hemochromatosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    143918018 Hemochromatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    143918018 Hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    143921016 Bronzed cirrhosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    143921016 Bronzed cirrhosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    143922011 Pigmentary cirrhosis of liver en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    143922011 Pigmentary cirrhosis of liver en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    143923018 von Recklinghausen-Appelbaum disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    143924012 Iron storage disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    143924012 Iron storage disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507253013 Familial hemochromatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    507253013 Familial hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507254019 Hereditary hemochromatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    507254019 Hereditary hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507255018 Primary hemochromatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    507255018 Primary hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507256017 Idiopathic hemochromatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    507256017 Idiopathic hemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507257014 Familial haemochromatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    507257014 Familial haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507258016 Hereditary haemochromatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    507258016 Hereditary haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507259012 Idiopathic haemochromatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    507259012 Idiopathic haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507260019 Primary haemochromatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    507260019 Primary haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507261015 Bronzed diabetes en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    507261015 Bronzed diabetes en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    507262010 von Recklinghausen-Applebaum disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    507263017 Haemochromatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    507263017 Haemochromatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    829117016 Hemochromatosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    829117016 Hemochromatosis (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
    Hemochromatosis Is a Iron overload (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Hemochromatosis Is a Metabolic and genetic disorder affecting the liver false Inferred relationship Existential restriction modifier (core metadata concept)
    Hemochromatosis Finding site Liver structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    Hemochromatosis Causative agent (attribute) Iron (substance) false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Hereditary hemochromatosis Is a False Hemochromatosis Inferred relationship Existential restriction modifier (core metadata concept)
    Juvenile hemochromatosis Is a False Hemochromatosis Inferred relationship Existential restriction modifier (core metadata concept)
    Secondary hemochromatosis Is a False Hemochromatosis Inferred relationship Existential restriction modifier (core metadata concept)
    Restrictive cardiomyopathy secondary to hemochromatosis Is a False Hemochromatosis Inferred relationship Existential restriction modifier (core metadata concept)
    Neonatal hemochromatosis (disorder) Is a False Hemochromatosis Inferred relationship Existential restriction modifier (core metadata concept)
    Dilated cardiomyopathy secondary to haemochromatosis Is a False Hemochromatosis Inferred relationship Existential restriction modifier (core metadata concept)

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

    SAME AS association reference set (foundation metadata concept)

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