Hemophagocytic Lymphohistiocytosis

Alias:
Lymphohistiocytosis, Hemophagocytic
Haemophagocytic Syndrome
Histiocytoses of Mononuclear Phagocytes
Haemophagocytic Lymphohistiocytosis Nos
Familial Hemophagocytic Lymphocytosis
Lymphohistiocytosis Hemophagocytic
Hemophagocytic Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hemophagocytic Lymphohistiocytosis, also known as lymphohistiocytosis, hemophagocytic, is related to hemophagocytic lymphohistiocytosis, familial, 1 and hemophagocytic lymphohistiocytosis, familial, 4, and has symptoms including ataxia, hemiplegia and icterus. An important gene associated with Hemophagocytic Lymphohistiocytosis is UNC13D (Unc-13 Homolog D), and among its related pathways/superpathways are Akt Signaling and Cytokine Signaling in Immune system. The drugs Dexamethasone and Dexamethasone acetate have been mentioned in the context of this disorder. Affiliated tissues include bone marrow and t cells, and related phenotypes are growth/size/body region and cellular
Related ID:
MESH:D051359
ICD11:1523519942

Basic Information

Inheritance
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Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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Medical Symptom

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Gene & Mutation

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References Literature

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