Code System Concept

Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Code System Concept

Code System Concept Code	398250003
Code System Concept Name	Familial hemophagocytic lymphohistiocytosis (disorder)
Code System Preferred Concept Name	Familial hemophagocytic lymphohistiocytosis (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Superseded By Concept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	07/31/2003
SDO Date Created	07/31/2003
SDO Date Revised	07/31/2003
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
1773209019	Familial haemophagocytic lymphohistiocytosis	Active	Synonym	false	false
1774495010	Familial hemophagocytic lymphohistiocytosis	Active	Synonym	false	false
1783629016	Familial haemophagocytic reticulosis	Active	Synonym	false	false
1783630014	FHL - Familial haemophagocytic lymphohistiocytosis	Active	Synonym	false	false
1783631013	Familial haemophagocytic histiocytosis	Active	Synonym	false	false
1784018010	Familial hemophagocytic reticulosis	Active	Synonym	false	false
1784019019	Familial hemophagocytic histiocytosis	Active	Synonym	false	false
1784020013	FHL - Familial hemophagocytic lymphohistiocytosis	Active	Synonym	false	false
1786183011	Familial histiocytic reticulosis	Active	Synonym	false	false
1786184017	Familial erythrophagocytic lymphohistiocytosis	Active	Synonym	false	false
1786185016	FEL - Familial erythrophagocytic lymphohistiocytosis	Active	Synonym	false	false
3701453010	Genetic haemophagocytic lymphohistiocytosis	Active	Synonym	false	false
3701454016	Primary haemophagocytic lymphohistiocytosis	Active	Synonym	false	false
3701455015	Genetic hemophagocytic lymphohistiocytosis	Active	Synonym	false	false
3701456019	Primary hemophagocytic lymphohistiocytosis	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
Immunosuppressed Condition	6 , 5 , 4 , 3 , 2 , 1
NAACCR SNOMEDCT Cancer Reportability List	1
Problem Value Set	3 , 2

Parent Concepts

Parent Concepts

Parent/Child (Relationship Type)

Atypical lymphoproliferative disorder (disorder) {20991001 , SNOMED-CT } Autosomal recessive hereditary disorder (disorder) {85995004 , SNOMED-CT } Disorder of hematopoietic structure (disorder) {414027002 , SNOMED-CT } Familial disease (disorder) {111941005 , SNOMED-CT } Hemolytic erythrophagocytic syndrome (disorder) {234436001 , SNOMED-CT } Hemophagocytic lymphohistiocytosis (disorder) {234437005 , SNOMED-CT } Hemophagocytic syndrome (disorder) {127069007 , SNOMED-CT } Hereditary white blood cell disorder (disorder) {414395005 , SNOMED-CT }

Other Relationships

No other relationships present.

Child Concepts

No child concepts present.

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