SettingsImmune system disorders
AIDS
Acquired immune deficiency syndrome or acquired immunodeficiency syndrome is a disease of the human immune system caused by the human immunodeficiency virus.
Acquired immune deficiency syndrome or acquired immunodeficiency syndrome is a disease of the human immune system caused by the human immunodeficiency virus.
AIDS-associated Kaposi sarcoma
AIDS-associated Kaposi sarcoma or KS-AIDS presents with cutaneous lesions that begin as one or several red to purple-red macules, rapidly progressing to papules, nodules, and plaques, with...
AIDS-associated Kaposi sarcoma or KS-AIDS presents with cutaneous lesions that begin as one or several red to purple-red macules, rapidly progressing to papules, nodules, and plaques, with...
Alternative names for chronic fatigue syndrome
Chronic fatigue syndrome (CFS) is the name currently used by the majority of the medical and scientific community to describe a condition or set of conditions characterized by fatigue and ...
Chronic fatigue syndrome (CFS) is the name currently used by the majority of the medical and scientific community to describe a condition or set of conditions characterized by fatigue and ...
Animal allergy
In medicine, animal allergy is hypersensitivity to certain substances produced by animals, such as the proteins in animal hair and saliva.
In medicine, animal allergy is hypersensitivity to certain substances produced by animals, such as the proteins in animal hair and saliva.
Arthus reaction
In immunology, the Arthus reaction is a type of local type III hypersensitivity reaction.
In immunology, the Arthus reaction is a type of local type III hypersensitivity reaction.
Asplenia
Asplenia refers to the absence of normal spleen function and is associated with some serious infection risks.
Asplenia refers to the absence of normal spleen function and is associated with some serious infection risks.
Atopy
Atopy (; Greek ἀτοπία - placelessness, out of place, special, unusual) or atopic syndrome is a predisposition toward developing certain allergic hypersensitivity reactions.
Atopy (; Greek ἀτοπία - placelessness, out of place, special, unusual) or atopic syndrome is a predisposition toward developing certain allergic hypersensitivity reactions.
Autoimmune heart disease
Autoimmune heart diseases are the effects of the body's own immune defense system mistaking cardiac antigens as foreign and attacking them leading to inflammation of the heart as a whole, or in ...
Autoimmune heart diseases are the effects of the body's own immune defense system mistaking cardiac antigens as foreign and attacking them leading to inflammation of the heart as a whole, or in ...
Autosplenectomy
An autosplenectomy (from 'auto-' self, '-splen-' spleen, '-ectomy' removal) occurs when a disease damages the spleen to such an extent that it is non-functioning and so equivalent to...
An autosplenectomy (from 'auto-' self, '-splen-' spleen, '-ectomy' removal) occurs when a disease damages the spleen to such an extent that it is non-functioning and so equivalent to...
Castleman's disease
Castleman's disease is a very rare disorder characterized by non-cancerous growths that may develop in the lymph node tissue at a single site or throughout the body.
Castleman's disease is a very rare disorder characterized by non-cancerous growths that may develop in the lymph node tissue at a single site or throughout the body.
Chronic fatigue syndrome
Chronic fatigue syndrome is the most common name used to designate a significantly debilitating medical disorder or group of disorders generally defined by persistent fatigue accompanied by oth...
Chronic fatigue syndrome is the most common name used to designate a significantly debilitating medical disorder or group of disorders generally defined by persistent fatigue accompanied by oth...
Chronic fatigue syndrome treatment
Treatment of chronic fatigue syndrome (CFS) is variable and uncertain, and the condition is primarily managed rather than cured.
Treatment of chronic fatigue syndrome (CFS) is variable and uncertain, and the condition is primarily managed rather than cured.
Chronic granulomatous disease
Chronic granulomatous disease (CGD) (also known as Bridges–Good syndrome, Chronic granulomatous disorder, and Quie syndrome) is a diverse group of hereditary diseases in which ...
Chronic granulomatous disease (CGD) (also known as Bridges–Good syndrome, Chronic granulomatous disorder, and Quie syndrome) is a diverse group of hereditary diseases in which ...
Clinical descriptions of chronic fatigue syndrome
The clinical descriptions of chronic fatigue syndrome (CFS) vary.
The clinical descriptions of chronic fatigue syndrome (CFS) vary.
Congenital disorder of glycosylation type IIc
Congenital disorder of glycosylation type IIc or Leukocyte adhesion deficiency-2 (LAD-2) is a type of leukocyte adhesion deficiency attributable to the absence of neutrophil sialyl-LewisX,...
Congenital disorder of glycosylation type IIc or Leukocyte adhesion deficiency-2 (LAD-2) is a type of leukocyte adhesion deficiency attributable to the absence of neutrophil sialyl-LewisX,...
Controversies related to chronic fatigue syndrome
Chronic fatigue syndrome is an illness with a long history of controversies.
Chronic fatigue syndrome is an illness with a long history of controversies.
Cryofibrinogenemia
Cryofibrinogenemia is defined by the presence of circulating cold insoluble complexes of fibrin, fibrinogen, fibronectin, and fibrin split products with albumin, immunoglobulins and plasma prote...
Cryofibrinogenemia is defined by the presence of circulating cold insoluble complexes of fibrin, fibrinogen, fibronectin, and fibrin split products with albumin, immunoglobulins and plasma prote...
Cutaneous small-vessel vasculitis
Cutaneous small-vessel vasculitis (also known as "Cutaneous leukocytoclastic angiitis," "Cutaneous leukocytoclastic vasculitis," "Cutaneous necrotizing venulitis," and "Hypersensitivity angiitis...
Cutaneous small-vessel vasculitis (also known as "Cutaneous leukocytoclastic angiitis," "Cutaneous leukocytoclastic vasculitis," "Cutaneous necrotizing venulitis," and "Hypersensitivity angiitis...
Cytokine release syndrome
Cytokine release syndrome is a common immediate complication occurring with the use of anti-T cell antibody infusions such as ATG, OKT3 and TGN1412.
Cytokine release syndrome is a common immediate complication occurring with the use of anti-T cell antibody infusions such as ATG, OKT3 and TGN1412.
Cytokine storm
A cytokine storm, or hypercytokinemia is a potentially fatal immune reaction consisting of a positive feedback loop between cytokines and immune cells, with highly elevated levels of vario...
A cytokine storm, or hypercytokinemia is a potentially fatal immune reaction consisting of a positive feedback loop between cytokines and immune cells, with highly elevated levels of vario...
Dennie-Morgan fold
A Dennie–Morgan fold, also known as a Dennie–Morgan line or an infraorbital fold, is a fold or line in the skin below the lower eyelid caused by edema in atopic dermatitis.
A Dennie–Morgan fold, also known as a Dennie–Morgan line or an infraorbital fold, is a fold or line in the skin below the lower eyelid caused by edema in atopic dermatitis.
Dennie–Morgan fold
A Dennie–Morgan fold, also known as a Dennie–Morgan line or an infraorbital fold, is a fold or line in the skin below the lower eyelid caused by edema in atopic dermatitis.
A Dennie–Morgan fold, also known as a Dennie–Morgan line or an infraorbital fold, is a fold or line in the skin below the lower eyelid caused by edema in atopic dermatitis.
DiGeorge syndrome
22q11.2 deletion syndrome, which has several presentations including DiGeorge syndrome, DiGeorge anomaly, velo-cardio-facial syndrome, Shprintzen syndrome, conotruncal anomaly face synd...
22q11.2 deletion syndrome, which has several presentations including DiGeorge syndrome, DiGeorge anomaly, velo-cardio-facial syndrome, Shprintzen syndrome, conotruncal anomaly face synd...
Dysgammaglobulinemia
Dysgammaglobulinemia is a type of immune disorder characterized by a reduction in some types of gamma globulins.
Dysgammaglobulinemia is a type of immune disorder characterized by a reduction in some types of gamma globulins.
Ectopic thymus
Ectopic thymus is a condition where thymus tissue is found in an abnormal location.
Ectopic thymus is a condition where thymus tissue is found in an abnormal location.
Erdheim–Chester disease
Erdheim–Chester disease (also known as Erdheim–Chester syndrome or polyostotic sclerosing histiocytosis) is a rare disease characterized by the abnormal multiplication of a specific ...
Erdheim–Chester disease (also known as Erdheim–Chester syndrome or polyostotic sclerosing histiocytosis) is a rare disease characterized by the abnormal multiplication of a specific ...
Extracutaneous mastocytoma
Extracutaneous mastocytoma presents with benign appearing mast cells occurring in sites other than the skin or bone marrow.
Extracutaneous mastocytoma presents with benign appearing mast cells occurring in sites other than the skin or bone marrow.
Foreign body granuloma
The foreign body granuloma is a response of biological tissue to any foreign material in the tissue.
The foreign body granuloma is a response of biological tissue to any foreign material in the tissue.
Garlic allergy
Garlic allergy or allergic contact dermatitis to garlic is a common inflammatory skin condition caused by contact with garlic oil or dust.
Garlic allergy or allergic contact dermatitis to garlic is a common inflammatory skin condition caused by contact with garlic oil or dust.
Gleich's syndrome
Gleich's syndrome or episodic angioedema with eosinophilia is a rare disease in which the body swells up episodically (angioedema), associated with raised antibodies of the IgM type and in...
Gleich's syndrome or episodic angioedema with eosinophilia is a rare disease in which the body swells up episodically (angioedema), associated with raised antibodies of the IgM type and in...
Gluten sensitivity
Gluten sensitivity (also gluten intolerance) is a spectrum of disorders, including celiac disease and wheat allergy, in which gluten has an adverse effect on the body.
Gluten sensitivity (also gluten intolerance) is a spectrum of disorders, including celiac disease and wheat allergy, in which gluten has an adverse effect on the body.
Gluten-sensitive enteropathy associated conditions
Gluten-sensitive enteropathy has key symptoms typically restricted to the bowel and associated tissues, however there are a wide variety of associated conditions.
Gluten-sensitive enteropathy has key symptoms typically restricted to the bowel and associated tissues, however there are a wide variety of associated conditions.
Gluten-sensitive idiopathic neuropathies
Diagnosis of gluten-sensitive neuropathies without a clear cause is on the rise.
Diagnosis of gluten-sensitive neuropathies without a clear cause is on the rise.
Graft-versus-host disease
Graft-versus-host disease is a common complication following an allogeneic tissue transplant.
Graft-versus-host disease is a common complication following an allogeneic tissue transplant.
Gulf War syndrome
Gulf War syndrome or Gulf War illness is a chronic multisymptom disorder affecting veterans and civilians after the 1991 Gulf War.
Gulf War syndrome or Gulf War illness is a chronic multisymptom disorder affecting veterans and civilians after the 1991 Gulf War.
Heavy chain disease
Heavy chain disease is a form of paraproteinemia with a proliferation of cells producing immunoglobulin heavy chains.
Heavy chain disease is a form of paraproteinemia with a proliferation of cells producing immunoglobulin heavy chains.
Helminthic therapy
Helminthic therapy, a type of immunotherapy, is the treatment of autoimmune diseases and immune disorders by means of deliberate infestation with a helminth or with the ova of a helminth.
Helminthic therapy, a type of immunotherapy, is the treatment of autoimmune diseases and immune disorders by means of deliberate infestation with a helminth or with the ova of a helminth.
History of chronic fatigue syndrome
The history of chronic fatigue syndrome is thought to date back to the 19th century and before.
The history of chronic fatigue syndrome is thought to date back to the 19th century and before.
HLA-B27
Human Leukocyte Antigen B27 is a class I surface antigen encoded by the B locus in the major histocompatibility complex on chromosome 6 and presents antigenic peptides to T cells.
Human Leukocyte Antigen B27 is a class I surface antigen encoded by the B locus in the major histocompatibility complex on chromosome 6 and presents antigenic peptides to T cells.
Hyper-IgM syndrome type 1
Hyper IgM Syndrome Type 1 is the X-linked variant of the Hyper-IgM syndrome.
Hyper IgM Syndrome Type 1 is the X-linked variant of the Hyper-IgM syndrome.
Hyper-IgM syndrome type 5
The fifth type of hyper-IgM syndrome has been characterized in three patients from France and Japan.
The fifth type of hyper-IgM syndrome has been characterized in three patients from France and Japan.
Hypergammaglobulinemia
Hypergammaglobulinemia is a medical condition with elevated levels of gamma globulin.
Hypergammaglobulinemia is a medical condition with elevated levels of gamma globulin.
Hyperimmunoglobulin E syndrome
Hyperimmunoglobulin E syndrome (HIES), also called Job's syndrome and Buckley syndrome, is a heterogeneous group of immune disorders.
Hyperimmunoglobulin E syndrome (HIES), also called Job's syndrome and Buckley syndrome, is a heterogeneous group of immune disorders.
Hypersensitivity
Hypersensitivity (also called hypersensitivity reaction) refers to undesirable reactions produced by the normal immune system.
Hypersensitivity (also called hypersensitivity reaction) refers to undesirable reactions produced by the normal immune system.
Hypogammaglobulinemia
Hypogammaglobulinemia is a type of immune disorder characterized by a reduction in all types of gamma globulins.
Hypogammaglobulinemia is a type of immune disorder characterized by a reduction in all types of gamma globulins.
Ichthyosis acquisita
Ichthyosis acquisita (or "acquired ichthyosis") is a disorder clinically and histologically similar to ichthyosis vulgaris.
Ichthyosis acquisita (or "acquired ichthyosis") is a disorder clinically and histologically similar to ichthyosis vulgaris.
Idiopathic CD4+ lymphocytopenia
Idiopathic CD4+ lymphocytopenia (ICL) is a very rare medical syndrome in which the body has too few CD4+ T lymphocytes, which are a kind of white blood cell.
Idiopathic CD4+ lymphocytopenia (ICL) is a very rare medical syndrome in which the body has too few CD4+ T lymphocytes, which are a kind of white blood cell.
IgG deficiency
IgG deficiency (Selective deficiency of immunoglobulin G) is a form of dysgammaglobulinemia where the proportional levels of IgG are reduced relative to other immunoglobulin.
IgG deficiency (Selective deficiency of immunoglobulin G) is a form of dysgammaglobulinemia where the proportional levels of IgG are reduced relative to other immunoglobulin.
Immune disorder
An immune disorder is a dysfunction of the immune system.
An immune disorder is a dysfunction of the immune system.
Immune reconstitution inflammatory syndrome
Immune reconstitution inflammatory syndrome (also known as "Immune recovery syndrome") is a condition seen in some cases of AIDS or immunosuppression, in which the immune system begins to recove...
Immune reconstitution inflammatory syndrome (also known as "Immune recovery syndrome") is a condition seen in some cases of AIDS or immunosuppression, in which the immune system begins to recove...
Immune-mediated disease
Immune-mediated diseases are conditions which result from abnormal activity of the body's immune system.
Immune-mediated diseases are conditions which result from abnormal activity of the body's immune system.
Immune-mediated inflammatory diseases
An immune-mediated inflammatory disease (IMID) is any of a group of conditions or diseases that lack a definitive etiology, but which are characterized by common inflammatory pathways lead...
An immune-mediated inflammatory disease (IMID) is any of a group of conditions or diseases that lack a definitive etiology, but which are characterized by common inflammatory pathways lead...
Immunodeficiency
Immunodeficiency is a state in which the immune system's ability to fight infectious disease is compromised or entirely absent.
Immunodeficiency is a state in which the immune system's ability to fight infectious disease is compromised or entirely absent.
Immunoproliferative disorder
Immunoproliferative disorders (also known as “immunoproliferative diseases” or “immunoproliferative neoplasms”) are disorders of the immune system that are characterized by the abnormal prolifer...
Immunoproliferative disorders (also known as “immunoproliferative diseases” or “immunoproliferative neoplasms”) are disorders of the immune system that are characterized by the abnormal prolifer...
Leukocyte adhesion deficiency
Leukocyte adhesion deficiency (LAD), is a rare autosomal recessive disorder characterized by immunodeficiency resulting in recurrent infections.
Leukocyte adhesion deficiency (LAD), is a rare autosomal recessive disorder characterized by immunodeficiency resulting in recurrent infections.
Leukocyte adhesion deficiency-1
Leukocyte adhesion deficiency-1 is a rare and often fatal genetic disorder in humans.
Leukocyte adhesion deficiency-1 is a rare and often fatal genetic disorder in humans.
Lymphocytopenia
Lymphocytopenia, or lymphopenia, is the condition of having an abnormally low level of lymphocytes in the blood.
Lymphocytopenia, or lymphopenia, is the condition of having an abnormally low level of lymphocytes in the blood.
Lymphoproliferative disorders
Lymphoproliferative disorders (LPDs) refer to several conditions in which lymphocytes are produced in excessive quantities.
Lymphoproliferative disorders (LPDs) refer to several conditions in which lymphocytes are produced in excessive quantities.
Mastocytosis
Mastocytosis is a group of rare disorders of both children and adults caused by the presence of too many mast cells and CD34+ mast cell precursors in a person's body.
Mastocytosis is a group of rare disorders of both children and adults caused by the presence of too many mast cells and CD34+ mast cell precursors in a person's body.
MonoMAC
The autosomal dominant syndrome associated with monocytopenia, B and NK cell lymphopenia and mycobacterial, fungal and viral infections (abbreviated MonoMAC) is a rare genetic disorder first des...
The autosomal dominant syndrome associated with monocytopenia, B and NK cell lymphopenia and mycobacterial, fungal and viral infections (abbreviated MonoMAC) is a rare genetic disorder first des...
Mortimer's disease
Mortimer's disease is a skin disease characterized by red blotchy patterns appearing all over the face and hands, and spreading through the body in an almost symmetrical pattern.
Mortimer's disease is a skin disease characterized by red blotchy patterns appearing all over the face and hands, and spreading through the body in an almost symmetrical pattern.
Multiple Myeloma Research Foundation
The Multiple Myeloma Research Foundation (MMRF) is a charitable organization dedicated to multiple myeloma, an incurable but treatable blood cancer, which afflicts over fifty thousand Americans ...
The Multiple Myeloma Research Foundation (MMRF) is a charitable organization dedicated to multiple myeloma, an incurable but treatable blood cancer, which afflicts over fifty thousand Americans ...
Myeloperoxidase deficiency
Myeloperoxidase deficiency is a common genetic disorder featuring deficiency, either in quantity or function, of myeloperoxidase, an enzyme found in certain phagocytic immune cells, especially p...
Myeloperoxidase deficiency is a common genetic disorder featuring deficiency, either in quantity or function, of myeloperoxidase, an enzyme found in certain phagocytic immune cells, especially p...
Opportunistic infection
An opportunistic infection is an infection caused by pathogens, particularly opportunistic pathogens that usually do not cause disease in a healthy host, i.e. one with a healthy immune system.
An opportunistic infection is an infection caused by pathogens, particularly opportunistic pathogens that usually do not cause disease in a healthy host, i.e. one with a healthy immune system.
Oral allergy syndrome
Oral allergy syndrome or OAS is a type of food allergy classified by a cluster of allergic reactions in the mouth in response to eating certain fruits, nuts, and vegetables that typically ...
Oral allergy syndrome or OAS is a type of food allergy classified by a cluster of allergic reactions in the mouth in response to eating certain fruits, nuts, and vegetables that typically ...
Paraneoplastic syndrome
Discovered by Dr. Nathan Pearson in 1989, A paraneoplastic syndrome is a disease or symptom that is the consequence of the presence of cancer in the body, but is not due to the local presence of...
Discovered by Dr. Nathan Pearson in 1989, A paraneoplastic syndrome is a disease or symptom that is the consequence of the presence of cancer in the body, but is not due to the local presence of...
Pathophysiology of chronic fatigue syndrome
The pathophysiology of chronic fatigue syndrome is unknown.
The pathophysiology of chronic fatigue syndrome is unknown.
Persistent polyclonal B-cell lymphocytosis
Persistent polyclonal B-cell lymphocytosis (PPBL) is very rare anomaly of the human immune system characterized by mild leukocytosis, chronic stable absolute polyclonal b-cell lymphocytosis, ele...
Persistent polyclonal B-cell lymphocytosis (PPBL) is very rare anomaly of the human immune system characterized by mild leukocytosis, chronic stable absolute polyclonal b-cell lymphocytosis, ele...
Pityriasis lichenoides chronica
Pityriasis lichenoides chronica (also known as "Chronic guttate parapsoriasis," "Chronic pityriasis lichenoides," "Dermatitis psoriasiformis nodularis," "Parapsoriasis chronica," and "Parapsoria...
Pityriasis lichenoides chronica (also known as "Chronic guttate parapsoriasis," "Chronic pityriasis lichenoides," "Dermatitis psoriasiformis nodularis," "Parapsoriasis chronica," and "Parapsoria...
Pityriasis lichenoides et varioliformis acuta
Pityriasis lichenoides et varioliformis acuta (also known as "Acute guttate parapsoriasis," "Acute parapsoriasis," "Acute pityriasis lichenoides," "Mucha-Habermann disease," "Parapsoriasis acuta...
Pityriasis lichenoides et varioliformis acuta (also known as "Acute guttate parapsoriasis," "Acute parapsoriasis," "Acute pityriasis lichenoides," "Mucha-Habermann disease," "Parapsoriasis acuta...
Plasmapheresis
Plasmapheresis (from the Greek πλάσμα—plasma, something molded, and ἀφαίρεσις—aphairesis, taking away) is the removal, treatment, and return of (components of) blood plasma from blood ci...
Plasmapheresis (from the Greek πλάσμα—plasma, something molded, and ἀφαίρεσις—aphairesis, taking away) is the removal, treatment, and return of (components of) blood plasma from blood ci...
Post-viral fatigue syndrome
Post-viral fatigue syndrome (PVFS) is a condition or conditions characterized by fatigue following a viral infection.
Post-viral fatigue syndrome (PVFS) is a condition or conditions characterized by fatigue following a viral infection.
Seabather's eruption
Seabather's eruption is a pruritic dermatitis caused by a hypersensitivity reaction to the immature nematocysts of larval-stage thimble jellyfish (Linuche unguiculata), sea anemones (Edwar...
Seabather's eruption is a pruritic dermatitis caused by a hypersensitivity reaction to the immature nematocysts of larval-stage thimble jellyfish (Linuche unguiculata), sea anemones (Edwar...
Selective immunoglobulin A deficiency
Immunoglobulin A deficiency, or IgA deficiency, is defined as decreased or absent level of serum IgA in the presence of normal serum levels of IgG and IgM in a patient older than 4 years o...
Immunoglobulin A deficiency, or IgA deficiency, is defined as decreased or absent level of serum IgA in the presence of normal serum levels of IgG and IgM in a patient older than 4 years o...
Systemic inflammatory response syndrome
In medicine, systemic inflammatory response syndrome (SIRS) is an inflammatory state affecting the whole body, frequently a response of the immune system to infection, but not necessarily so.
In medicine, systemic inflammatory response syndrome (SIRS) is an inflammatory state affecting the whole body, frequently a response of the immune system to infection, but not necessarily so.
Thymus hyperplasia
Thymus hyperplasia (or thymic hyperplasia) refers to an enlargent ("hyperplasia") of the thymus.
Thymus hyperplasia (or thymic hyperplasia) refers to an enlargent ("hyperplasia") of the thymus.
Transplant rejection
Transplant rejection occurs when a transplanted animal tissue is rejected by the recipient's immune system, which destroys the transplanted material.
Transplant rejection occurs when a transplanted animal tissue is rejected by the recipient's immune system, which destroys the transplanted material.
Type I hypersensitivity
Type I hypersensitivity (or immediate hypersensitivity) is an allergic reaction provoked by reexposure to a specific type of antigen referred to as an allergen.
Type I hypersensitivity (or immediate hypersensitivity) is an allergic reaction provoked by reexposure to a specific type of antigen referred to as an allergen.
Type II hypersensitivity
In type II hypersensitivity (or cytotoxic hypersensitivity) the antibodies produced by the immune response bind to antigens on the patient's own cell surfaces.
In type II hypersensitivity (or cytotoxic hypersensitivity) the antibodies produced by the immune response bind to antigens on the patient's own cell surfaces.
Type III hypersensitivity
Type III hypersensitivity occurs when antigens and antibodies (IgG or IgM) are present in roughly equal amounts, causing extensive cross-linking.
Type III hypersensitivity occurs when antigens and antibodies (IgG or IgM) are present in roughly equal amounts, causing extensive cross-linking.
Type IV hypersensitivity
Type IV hypersensitivity is often called delayed type hypersensitivity as the reaction takes two to three days to develop.
Type IV hypersensitivity is often called delayed type hypersensitivity as the reaction takes two to three days to develop.
Viktor Mucha
Viktor Mucha was a dermatologist from Austria.
Viktor Mucha was a dermatologist from Austria.
Wiskott-Aldrich syndrome
Wiskott–Aldrich syndrome (WAS) is a rare X-linked recessive disease characterized by eczema, thrombocytopenia (low platelet count), immune deficiency, and bloody diarrhea (secondary to the throm...
Wiskott–Aldrich syndrome (WAS) is a rare X-linked recessive disease characterized by eczema, thrombocytopenia (low platelet count), immune deficiency, and bloody diarrhea (secondary to the throm...
Wiskott–Aldrich syndrome
Wiskott–Aldrich syndrome (WAS) is a rare X-linked recessive disease characterized by eczema, thrombocytopenia (low platelet count), immune deficiency, and bloody diarrhea (secondary to the throm...
Wiskott–Aldrich syndrome (WAS) is a rare X-linked recessive disease characterized by eczema, thrombocytopenia (low platelet count), immune deficiency, and bloody diarrhea (secondary to the throm...
ZAP70 deficiency
ZAP70 deficiency, or zeta-chain-associated protein 70 kD deficiency, is a rare autosomal recessive form of severe combined immunodeficiency (SCID).
ZAP70 deficiency, or zeta-chain-associated protein 70 kD deficiency, is a rare autosomal recessive form of severe combined immunodeficiency (SCID).