Familial hemophagocytic lymphohistiocytosis 398250003

SNOMED CT code

SNOMED code

398250003

name

Familial hemophagocytic lymphohistiocytosis

status

active

date introduced

2003-07-31

fully specified name(s)

Familial hemophagocytic lymphohistiocytosis (disorder)

synonyms

Familial haemophagocytic lymphohistiocytosis
Familial hemophagocytic lymphohistiocytosis
Familial haemophagocytic reticulosis
FHL - Familial haemophagocytic lymphohistiocytosis
Familial haemophagocytic histiocytosis
Familial hemophagocytic reticulosis
Familial hemophagocytic histiocytosis
FHL - Familial hemophagocytic lymphohistiocytosis
Familial histiocytic reticulosis
Familial erythrophagocytic lymphohistiocytosis
FEL - Familial erythrophagocytic lymphohistiocytosis
Genetic haemophagocytic lymphohistiocytosis
Primary haemophagocytic lymphohistiocytosis
Genetic hemophagocytic lymphohistiocytosis
Primary hemophagocytic lymphohistiocytosis

attributes - group1

Finding site

Mononuclear phagocyte system structure 127908000

Associated morphology

Histiocytic proliferation 1186648002

Pathological process

Abnormal immune process 769247005

parents

Familial disease 111941005
Hemophagocytic lymphohistiocytosis 234437005
Hereditary white blood cell disorder 414395005
Autosomal recessive hereditary disorder 85995004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Familial disease 111941005
Familial hemophagocytic lymphohistiocytosis 398250003

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of body system 362965005
Disorder of hematopoietic structure 414027002
Hemophagocytic lymphohistiocytosis 234437005
Familial hemophagocytic lymphohistiocytosis 398250003

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of blood, lymphatics and immune system 299691001
Disorder of cellular component of blood 414022008
White blood cell disorder 54097007
Hereditary white blood cell disorder 414395005
Familial hemophagocytic lymphohistiocytosis 398250003

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Familial hemophagocytic lymphohistiocytosis 398250003

ancestors

sorted most to least specific

Familial disease 111941005
Hemophagocytic lymphohistiocytosis 234437005
Hereditary white blood cell disorder 414395005
Autosomal recessive hereditary disorder 85995004
Hemolytic erythrophagocytic syndrome 234436001
Hereditary disorder of immune system 363138005
Autosomal hereditary disorder 1899006
Disorder of hematopoietic structure 414027002
Hereditary disorder of cellular element of blood 414393003
Histiocytic syndrome 127068004
Hereditary disorder by system 363137000
Combined phagocytic defect 234591005
Disorder of hematopoietic morphology 414026006
Hereditary disease 32895009
Phagocytic cell dysfunction 302874002
Qualitative abnormality of granulocyte 319171004
Disorder of immune structure 414030009
Genetic disease 782964007
Disorder of body system 362965005
Phagocytic cell defect 234573000
White blood cell disorder 54097007
Primary immune deficiency disorder 58606001
Disorder of cellular component of blood 414022008
Immunodeficiency disorder 234532001
Finding of blood, lymphatics and immune system 299691001
Disorder of immune function 414029004
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Familial disease 111941005

Familial hemophagocytic lymphohistiocytosis 398250003

SNOMED CT code