35400008: Hereditary hemochromatosis (disorder)

SNOMED CT Concept\Clinical finding\Disease\...

\Genetic disease\Hereditary disease\Hereditary metabolic disease\Hereditary hemochromatosis

\Metabolic disease\Hereditary metabolic disease\Hereditary hemochromatosis
\Metabolic disease\Disorder of mineral metabolism\Disorder of iron metabolism\Iron overload\Hemochromatosis\Hereditary hemochromatosis

\Nutritional disorder\Disorder of hyperalimentation\Excess intake of micronutrients\Mineral excess\Iron overload\Hemochromatosis\Hereditary hemochromatosis

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

59062011 Hereditary hemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
59063018 Primary hemochromatosis en Synonym Inactive Only initial character case insensitive SNOMED CT core module
59064012 Idiopathic hemochromatosis en Synonym Inactive Only initial character case insensitive SNOMED CT core module
59065013 Familial hemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
486146014 Primary haemochromatosis en Synonym Inactive Only initial character case insensitive SNOMED CT core module
486147017 Hereditary haemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
486148010 Familial haemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
486149019 Idiopathic haemochromatosis en Synonym Inactive Only initial character case insensitive SNOMED CT core module
767034016 Hereditary 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
Hereditary hemochromatosis	Is a	Autosomal dominant hereditary disorder	false	Inferred relationship	Existential restriction modifier
Hereditary hemochromatosis	Is a	Digestive system hereditary disorder	false	Inferred relationship	Existential restriction modifier
Hereditary hemochromatosis	Is a	Hemochromatosis	false	Inferred relationship	Existential restriction modifier
Hereditary hemochromatosis	Finding site	Liver structure	false	Inferred relationship	Existential restriction modifier
Hereditary hemochromatosis	Causative agent	Iron	false	Inferred relationship	Existential restriction modifier
Hereditary hemochromatosis	Is a	Hemochromatosis	true	Inferred relationship	Existential restriction modifier
Hereditary hemochromatosis	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Hereditary hemochromatosis	Causative agent	Iron AND/OR iron compound	false	Inferred relationship	Existential restriction modifier
Hereditary hemochromatosis	Causative agent	Iron and/or iron compound	true	Inferred relationship	Existential restriction modifier	1
Hereditary hemochromatosis	Is a	Hereditary disease	false	Inferred relationship	Existential restriction modifier
Hereditary hemochromatosis	Is a	Hereditary metabolic disease	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hemochromatosis type 3	Is a	True	Hereditary hemochromatosis	Inferred relationship	Existential restriction modifier
Autosomal dominant hereditary hemochromatosis	Is a	True	Hereditary hemochromatosis	Inferred relationship	Existential restriction modifier
Juvenile hemochromatosis	Is a	True	Hereditary hemochromatosis	Inferred relationship	Existential restriction modifier
Hemochromatosis type 1	Is a	True	Hereditary hemochromatosis	Inferred relationship	Existential restriction modifier
Ferritin heavy chain 1-related iron overload	Is a	True	Hereditary hemochromatosis	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets