398250003: Familial hemophagocytic lymphohistiocytosis (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\...

\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Familial hemophagocytic lymphohistiocytosis

\White blood cell disorder\Hereditary white blood cell disorder\Familial hemophagocytic lymphohistiocytosis
\White blood cell disorder\Qualitative abnormality of granulocyte\Combined phagocytic defect\Hemolytic erythrophagocytic syndrome\Hemophagocytic lymphohistiocytosis\Familial hemophagocytic lymphohistiocytosis

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Familial hemophagocytic lymphohistiocytosis
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder\Familial hemophagocytic lymphohistiocytosis
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Familial hemophagocytic lymphohistiocytosis
\Disease\Disorder of immune function\Hereditary disorder of immune system\Hereditary white blood cell disorder\Familial hemophagocytic lymphohistiocytosis
\Disease\Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Phagocytic cell defect\Phagocytic cell dysfunction\Combined phagocytic defect\Hemolytic erythrophagocytic syndrome\Hemophagocytic lymphohistiocytosis\Familial hemophagocytic lymphohistiocytosis
\Disease\Disorder of immune function\White blood cell disorder\Hereditary white blood cell disorder\Familial hemophagocytic lymphohistiocytosis
\Disease\Disorder of immune function\White blood cell disorder\Qualitative abnormality of granulocyte\Combined phagocytic defect\Hemolytic erythrophagocytic syndrome\Hemophagocytic lymphohistiocytosis\Familial hemophagocytic lymphohistiocytosis
\Disease\Disorder of hematopoietic cell proliferation\Histiocytic syndrome\Hemolytic erythrophagocytic syndrome\Hemophagocytic lymphohistiocytosis\Familial hemophagocytic lymphohistiocytosis
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Familial hemophagocytic lymphohistiocytosis
\Disease\Disorder of cellular component of blood\White blood cell disorder\Hereditary white blood cell disorder\Familial hemophagocytic lymphohistiocytosis
\Disease\Disorder of cellular component of blood\White blood cell disorder\Qualitative abnormality of granulocyte\Combined phagocytic defect\Hemolytic erythrophagocytic syndrome\Hemophagocytic lymphohistiocytosis\Familial hemophagocytic lymphohistiocytosis
\Disease\Disorder of body system\Disorder of immune structure\Combined phagocytic defect\Hemolytic erythrophagocytic syndrome\Hemophagocytic lymphohistiocytosis\Familial hemophagocytic lymphohistiocytosis
\Disease\Disorder of body system\Disorder of hematopoietic structure\Hemophagocytic lymphohistiocytosis\Familial hemophagocytic lymphohistiocytosis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Familial hemophagocytic lymphohistiocytosis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder\Familial hemophagocytic lymphohistiocytosis
\Disease\Familial disease\Familial hemophagocytic lymphohistiocytosis

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

1766169019 Familial hemophagocytic lymphohistiocytosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

1773209019 Familial haemophagocytic lymphohistiocytosis en Synonym Active Entire term case insensitive SNOMED CT core module

1774495010 Familial hemophagocytic lymphohistiocytosis en Synonym Active Entire term case insensitive SNOMED CT core module

1783629016 Familial haemophagocytic reticulosis en Synonym Active Entire term case insensitive SNOMED CT core module

1783630014 FHL - Familial haemophagocytic lymphohistiocytosis en Synonym Active Entire term case sensitive SNOMED CT core module

1783631013 Familial haemophagocytic histiocytosis en Synonym Active Entire term case insensitive SNOMED CT core module

1784018010 Familial hemophagocytic reticulosis en Synonym Active Entire term case insensitive SNOMED CT core module

1784019019 Familial hemophagocytic histiocytosis en Synonym Active Entire term case insensitive SNOMED CT core module

1784020013 FHL - Familial hemophagocytic lymphohistiocytosis en Synonym Active Entire term case sensitive SNOMED CT core module

1786183011 Familial histiocytic reticulosis en Synonym Active Entire term case insensitive SNOMED CT core module

1786184017 Familial erythrophagocytic lymphohistiocytosis en Synonym Active Entire term case insensitive SNOMED CT core module

1786185016 FEL - Familial erythrophagocytic lymphohistiocytosis en Synonym Active Entire term case sensitive SNOMED CT core module

3701453010 Genetic haemophagocytic lymphohistiocytosis en Synonym Active Entire term case insensitive SNOMED CT core module

3701454016 Primary haemophagocytic lymphohistiocytosis en Synonym Active Entire term case insensitive SNOMED CT core module

3701455015 Genetic hemophagocytic lymphohistiocytosis en Synonym Active Entire term case insensitive SNOMED CT core module

3701456019 Primary hemophagocytic lymphohistiocytosis en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial hemophagocytic lymphohistiocytosis	Is a	Atypical lymphoproliferative disorder	false	Inferred relationship	Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis	Is a	Hemophagocytic syndrome	false	Inferred relationship	Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis	Is a	Hemolytic erythrophagocytic syndrome	false	Inferred relationship	Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis	Associated morphology	Immunoproliferative morphology	false	Inferred relationship	Existential restriction modifier	3
Familial hemophagocytic lymphohistiocytosis	Finding site	Leukocyte	false	Inferred relationship	Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis	Finding site	Lymphocytic tissue structure	false	Inferred relationship	Existential restriction modifier	2
Familial hemophagocytic lymphohistiocytosis	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier	1
Familial hemophagocytic lymphohistiocytosis	Finding site	Structure of immune system	false	Inferred relationship	Existential restriction modifier	3
Familial hemophagocytic lymphohistiocytosis	Associated morphology	Proliferation	false	Inferred relationship	Existential restriction modifier	2
Familial hemophagocytic lymphohistiocytosis	Associated morphology	Histiocytosis	false	Inferred relationship	Existential restriction modifier	1
Familial hemophagocytic lymphohistiocytosis	Associated morphology	White blood cell abnormality	false	Inferred relationship	Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis	Is a	Disorder of hematopoietic structure	false	Inferred relationship	Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis	Associated morphology	Lymphoproliferative disorder	false	Inferred relationship	Existential restriction modifier	4
Familial hemophagocytic lymphohistiocytosis	Has definitional manifestation	Immune system finding	false	Inferred relationship	Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis	Finding site	Structure of immune system	false	Inferred relationship	Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis	Has definitional manifestation	White blood cell finding	false	Inferred relationship	Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis	Associated morphology	Histiocytosis	false	Inferred relationship	Existential restriction modifier	1
Familial hemophagocytic lymphohistiocytosis	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier	1
Familial hemophagocytic lymphohistiocytosis	Has definitional manifestation	Immune system finding	false	Inferred relationship	Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis	Is a	Familial disease	true	Inferred relationship	Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis	Finding site	Mononuclear phagocyte system structure	false	Inferred relationship	Existential restriction modifier	2
Familial hemophagocytic lymphohistiocytosis	Is a	Hemophagocytic lymphohistiocytosis	true	Inferred relationship	Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis	Pathological process	Abnormal immune process	false	Inferred relationship	Existential restriction modifier	3
Familial hemophagocytic lymphohistiocytosis	Pathological process	Abnormal immune process	false	Inferred relationship	Existential restriction modifier	2
Familial hemophagocytic lymphohistiocytosis	Associated morphology	Histiocytic proliferation - category	false	Inferred relationship	Existential restriction modifier	2
Familial hemophagocytic lymphohistiocytosis	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis	Is a	Hereditary white blood cell disorder	true	Inferred relationship	Existential restriction modifier
Familial hemophagocytic lymphohistiocytosis	Finding site	Mononuclear phagocyte system structure	true	Inferred relationship	Existential restriction modifier	1
Familial hemophagocytic lymphohistiocytosis	Associated morphology	Histiocytic proliferation	true	Inferred relationship	Existential restriction modifier	1
Familial hemophagocytic lymphohistiocytosis	Pathological process	Abnormal immune process	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
1766169019	Familial hemophagocytic lymphohistiocytosis (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
1773209019	Familial haemophagocytic lymphohistiocytosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1774495010	Familial hemophagocytic lymphohistiocytosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1783629016	Familial haemophagocytic reticulosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1783630014	FHL - Familial haemophagocytic lymphohistiocytosis	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
1783631013	Familial haemophagocytic histiocytosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1784018010	Familial hemophagocytic reticulosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1784019019	Familial hemophagocytic histiocytosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1784020013	FHL - Familial hemophagocytic lymphohistiocytosis	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
1786183011	Familial histiocytic reticulosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1786184017	Familial erythrophagocytic lymphohistiocytosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1786185016	FEL - Familial erythrophagocytic lymphohistiocytosis	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3701453010	Genetic haemophagocytic lymphohistiocytosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3701454016	Primary haemophagocytic lymphohistiocytosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3701455015	Genetic hemophagocytic lymphohistiocytosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3701456019	Primary hemophagocytic lymphohistiocytosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module