1230310007: Ferritin heavy chain 1-related iron overload (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Liver finding\Disorder of liver\Metabolic and genetic disorder affecting the liver\Ferritin heavy chain 1-related iron overload

\Digestive system finding\Liver finding\Disorder of liver\Metabolic and genetic disorder affecting the liver\Ferritin heavy chain 1-related iron overload
\Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Ferritin heavy chain 1-related iron overload
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of liver\Metabolic and genetic disorder affecting the liver\Ferritin heavy chain 1-related iron overload

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Ferritin heavy chain 1-related iron overload
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Liver finding\Disorder of liver\Metabolic and genetic disorder affecting the liver\Ferritin heavy chain 1-related iron overload
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Ferritin heavy chain 1-related iron overload
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Ferritin heavy chain 1-related iron overload

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Hereditary hemochromatosis\Ferritin heavy chain 1-related iron overload
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Ferritin heavy chain 1-related iron overload
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Ferritin heavy chain 1-related iron overload
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Ferritin heavy chain 1-related iron overload
\Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Ferritin heavy chain 1-related iron overload
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Disorder of liver\Metabolic and genetic disorder affecting the liver\Ferritin heavy chain 1-related iron overload
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Ferritin heavy chain 1-related iron overload
\Disease\Metabolic disease\Hereditary metabolic disease\Hereditary hemochromatosis\Ferritin heavy chain 1-related iron overload
\Disease\Metabolic disease\Metabolic and genetic disorder affecting the liver\Ferritin heavy chain 1-related iron overload
\Disease\Metabolic disease\Disorder of mineral metabolism\Disorder of iron metabolism\Iron overload\Hemochromatosis\Hereditary hemochromatosis\Ferritin heavy chain 1-related iron overload
\Disease\Nutritional disorder\Disorder of hyperalimentation\Excess intake of micronutrients\Mineral excess\Iron overload\Hemochromatosis\Hereditary hemochromatosis\Ferritin heavy chain 1-related iron overload

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Jun 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

5068836018 FTH1-associated iron overload en Synonym Active Entire term case sensitive SNOMED CT core module

5068837010 Ferritin heavy chain 1-related iron overload en Synonym Active Entire term case insensitive SNOMED CT core module

5068838017 FTH1-related iron overload en Synonym Active Entire term case sensitive SNOMED CT core module

5068839013 FTH1 (ferritin heavy chain 1) related iron overload en Synonym Active Entire term case sensitive SNOMED CT core module

5068840010 Ferritin heavy chain 1-related iron overload (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
Ferritin heavy chain 1-related iron overload	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Ferritin heavy chain 1-related iron overload	Is a	Metabolic and genetic disorder affecting the liver	true	Inferred relationship	Existential restriction modifier
Ferritin heavy chain 1-related iron overload	Is a	Hereditary hemochromatosis	true	Inferred relationship	Existential restriction modifier
Ferritin heavy chain 1-related iron overload	Is a	Digestive system hereditary disorder	true	Inferred relationship	Existential restriction modifier
Ferritin heavy chain 1-related iron overload	Finding site	Liver structure	true	Inferred relationship	Existential restriction modifier	1
Ferritin heavy chain 1-related iron overload	Causative agent	Iron and/or iron compound	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
5068836018	FTH1-associated iron overload	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
5068837010	Ferritin heavy chain 1-related iron overload	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
5068838017	FTH1-related iron overload	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
5068839013	FTH1 (ferritin heavy chain 1) related iron overload	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
5068840010	Ferritin heavy chain 1-related iron overload (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module