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50855007: Juvenile hemochromatosis (disorder)

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

\Genetic disease\Hereditary disease\...

\Hereditary metabolic disease\Hereditary hemochromatosis\Juvenile hemochromatosis

\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Juvenile hemochromatosis

\Degenerative disorder\Juvenile hemochromatosis

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

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

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

84743011 Juvenile hemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module

495799017 Juvenile haemochromatosis en Synonym Active Entire term case insensitive SNOMED CT core module

788689013 Juvenile hemochromatosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

4643576013 Haemochromatosis type 2 en Synonym Active Entire term case insensitive SNOMED CT core module

4643577016 Hemochromatosis type 2 en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Juvenile hemochromatosis	Is a	Hemochromatosis	false	Inferred relationship	Existential restriction modifier
Juvenile hemochromatosis	Finding site	Liver structure	false	Inferred relationship	Existential restriction modifier
Juvenile hemochromatosis	Causative agent	Iron	false	Inferred relationship	Existential restriction modifier
Juvenile hemochromatosis	Occurrence	Childhood	false	Inferred relationship	Existential restriction modifier	2
Juvenile hemochromatosis	Is a	Hemochromatosis	false	Inferred relationship	Existential restriction modifier
Juvenile hemochromatosis	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Juvenile hemochromatosis	Causative agent	Iron AND/OR iron compound	false	Inferred relationship	Existential restriction modifier
Juvenile hemochromatosis	Causative agent	Iron and/or iron compound	true	Inferred relationship	Existential restriction modifier	1
Juvenile hemochromatosis	Is a	Hereditary hemochromatosis	true	Inferred relationship	Existential restriction modifier
Juvenile hemochromatosis	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Juvenile hemochromatosis	Is a	Degenerative disorder	true	Inferred relationship	Existential restriction modifier
Juvenile hemochromatosis	Occurrence	Childhood	true	Inferred relationship	Existential restriction modifier	1
Juvenile hemochromatosis	Associated morphology	Deposition of iron	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Type 2A juvenile hereditary hemochromatosis	Is a	True	Juvenile hemochromatosis	Inferred relationship	Existential restriction modifier
Type 2B juvenile hereditary hemochromatosis	Is a	True	Juvenile hemochromatosis	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
84743011	Juvenile hemochromatosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
495799017	Juvenile haemochromatosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
788689013	Juvenile hemochromatosis (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
4643576013	Haemochromatosis type 2	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4643577016	Hemochromatosis type 2	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module