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

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

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