Code System Concept

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Code System Concept

Code System Concept Code	35400008
Code System Concept Name	Hereditary hemochromatosis (disorder)
Code System Preferred Concept Name	Hereditary hemochromatosis (disorder)
Concept Status	Published
Concept Status Date	09/01/2024
Code System Name	SNOMED-CT

Concept Relationships
Concept Details

Concept Details

Code System Code	PH_SNOMED-CT
Code System OID	2.16.840.1.113883.6.96
HL7 Table 0396 Code	SCT
Superseded By Concept
SDO Concept Status	Active
SDO Concept Status Date	01/31/2020
SDO Date Created	01/31/2002
SDO Date Revised	01/31/2020
Description
Sequence

Extended Properties

No extended properties.

Concept Alternate Designations

SDO Designation ID	Concept Designation Description	Status	Designation Type	PHIN Preferred Term Flag	Code Flag
486146014	Primary haemochromatosis	Active	Synonym	false	false
486147017	Hereditary haemochromatosis	Active	Synonym	false	false
486148010	Familial haemochromatosis	Active	Synonym	false	false
486149019	Idiopathic haemochromatosis	Active	Synonym	false	false
59062011	Hereditary hemochromatosis	Active	Synonym	false	false
59063018	Primary hemochromatosis	Active	Synonym	false	false
59064012	Idiopathic hemochromatosis	Active	Synonym	false	false
59065013	Familial hemochromatosis	Active	Synonym	false	false

Associated Value Sets

Value Set Name	Version(s)
Clinical Finding (NNDSS)	2 , 1
Disease	10 , 9 , 8 , 7 , 6 , 5 , 4 , 3 , 2 , 1
Problem Value Set	3 , 2

Parent Concepts

Parent Concepts

Parent/Child (Relationship Type)

Autosomal dominant hereditary disorder (disorder) {11164009 , SNOMED-CT } Digestive system hereditary disorder (disorder) {363080007 , SNOMED-CT } Hemochromatosis (disorder) {399187006 , SNOMED-CT } Hemochromatosis (disorder) {86781004 , SNOMED-CT } Hereditary disease (disorder) {32895009 , SNOMED-CT } Hereditary metabolic disease (disorder) {1821000146108 , SNOMED-CT }

Other Relationships

No other relationships present.

Child Concepts

Hereditary hemochromatosis (disorder) {35400008 , SNOMED-CT }

Parent/Child (Relationship Type)

Autosomal dominant hereditary hemochromatosis (disorder) {719975002 , SNOMED-CT } Digenic hemochromatosis (disorder) {1299153008 , SNOMED-CT } Ferritin heavy chain 1-related iron overload (disorder) {1230310007 , SNOMED-CT } Ferroportin disease (disorder) {1303911001 , SNOMED-CT } Hemochromatosis type 1 (disorder) {1186847009 , SNOMED-CT } Hemochromatosis type 3 (disorder) {719974003 , SNOMED-CT } Juvenile hemochromatosis (disorder) {50855007 , SNOMED-CT } Solute carrier family 40 member 1-related hemochromatosis (disorder) {1303910000 , SNOMED-CT }

Page last reviewed:June 20, 2024
Page last updated:June 20, 2024
Content source:
- Centers for Disease Control and Prevention,