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Hemophagocytic Lymphohistiocytosis
Hemophagocytic lymphohistiocytosis
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Blood disorders
(8)
Acute monocytic leukemia
Diamond Blackfan anemia
Acquired hemolytic anemia
Acute lymphoblastic leukemia
Acute myeloid leukemia
Acute myeloid leukemia
Lymphomas
Neutropenia
Hematologic
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Hematology
Acquired pure red cell aplasia
Cytopenia
Bone marrow transplantation
Activated protein c resistance
Pancytopenia
Acquired hemolytic anemia
Autosomal recessive disorders
Griscelli syndrome
Niemann Pick disease
Sandhoff disease
Hermansky-Pudlak syndrome
Genetic disorders
(8)
Sideroblastic anemia
Severe combined immunodeficiency
Griscelli syndrome
Diamond Blackfan anemia
Niemann Pick disease
Niemann Pick disease
Sandhoff disease
Activated protein c resistance
Hermansky-Pudlak syndrome
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Diseases and disorders
(27)
Non-langerhans-cell histiocytosis
Sea-blue histiocyte syndrome
Follicular dendritic cell sarcoma
Lymphohistiocytosis
Erdheim-chester disease
Erdheim-chester disease
Histiocytes
Langerhans cell histiocytosis
Letterer-Siwe disease
Syndromes
X-linked lymphoproliferative syndrome
Scleromyxedema
Eosinophilic granuloma
Polychondritis
Primary amyloidosis
Graft versus host disease
Acquired pure red cell aplasia
Acute monocytic leukemia
Niemann Pick disease
Acute lymphoblastic leukemia
Acute myeloid leukemia
Sandhoff disease
Sideroblastic anemia
Activated protein c resistance
Lymphomas
Neutropenia
Hermansky-Pudlak syndrome
Severe combined immunodeficiency
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Neoplasm
Langerhans cell sarcoma
Interdigitating dendritic cell sarcoma
Histiocytic sarcoma
Mononuclear phagocytes
Monocytes
Dendritic cell
Histiocytes
Langerhans cell
Macrophages
Splenocyte
Noninfectious immunodeficiency-related cutaneous conditions
(26)
Bare lymphocyte syndrome
Cartilage–hair hypoplasia
Chediak–Higashi syndrome
Chronic granulomatous disease
Common variable immunodeficiency
Common variable immunodeficiency
Complement deficiency
Di George's syndrome
Graft versus host disease
Griscelli syndrome
Hyperimmunoglobulin E syndrome
Immunodeficiency with hyper-immu- noglobulin M
Immunoglobulin M deficiency
Leukocyte adhesion molecule deficiency
Myeloperoxidase deficiency
Neutropenia
Nezelof syndrome
Omenn syndrome
Purine nucleoside phosphorylase deficiency
Selective immunoglobulin A deficiency
Severe combined immunodeficiency
Thymoma with immunodeficiency
WHIM syndrome
Wiskott-Aldrich syndrome
X-linked agammaglobulinemia
X-linked hyper-immu- noglobulin M syndrome
X-linked lymphoproliferative syndrome
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Leukemia
(30)
Juvenile myelomonocytic leukemia
Accelerated phase chronic myelogenous leukemia
Acute basophilic leukemia
Acute eosinophilic leukemia
Acute erythroid leukemia
Acute erythroid leukemia
Acute lymphoblastic leukemia
Acute monocytic leukemia
Acute myeloblastic leukemia with maturation
Acute myeloid dendritic cell leukemia
Acute myeloid leukemia
Antileukemic drug
B-cell chronic lymphocytic leukemia
B-cell leukemia
B-cell prolymphocytic leukemia
Chronic myelogenous leukemia
Chronic myelomonocytic leukemia
Chronic neutrophilic leukemia
Hairy cell leukemia
Large granular lymphocytic leukemia
Lymphoid leukemia
Minimal residual disease
Minimally differentiated acute myeloblastic leukemia
Monocytic leukemia
Myeloid leukemia
Myelomonocyte
Plasma cell leukemia
Precursor B acute lymphoblastic leukemia/lymphoma
Prolymphocytic leukemia
T-cell leukemia
T-cell prolymphocytic leukemia
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See also
(20)
Juvenile xanthogranuloma
UNC13D
Macrophage- -activation syndrome
Malignant histiocytosis
PRF1
PRF1
STX11
Hereditary stomatocytosis
RAB27A
Hyperferritinemia
MACPF
Fludarabine
Membrane attack complex
Etoposide
Alternative names for chronic fatigue syndrome (Chronic Epstein-Barr virus)
Familial
Allogeneic
Systemic vasculitis
Lymphocytes
Friday Harbor Laboratories
Syntaxin
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