Autoimmune disease
Encyclopedia
Autoimmune diseases arise from an overactive immune response of the body against substances and tissues normally present in the body. In other words, the body actually attacks its own cells. The immune system mistakes some part of the body as a pathogen
Pathogen
A pathogen gignomai "I give birth to") or infectious agent — colloquially, a germ — is a microbe or microorganism such as a virus, bacterium, prion, or fungus that causes disease in its animal or plant host...

 and attacks it. This may be restricted to certain organ
Organ (anatomy)
In biology, an organ is a collection of tissues joined in structural unit to serve a common function. Usually there is a main tissue and sporadic tissues . The main tissue is the one that is unique for the specific organ. For example, main tissue in the heart is the myocardium, while sporadic are...

s (e.g. in autoimmune thyroiditis
Autoimmune thyroiditis
Autoimmune thyroiditis is a form of thyroiditis associated with an autoimmune disease where the body treats the thyroid gland and sometimes the hormones it produces as foreign bodies, therefore rejecting and attacking both.-Treatment:...

) or involve a particular tissue in different places (e.g. Goodpasture's disease which may affect the basement membrane
Basement membrane
The basement membrane is a thin sheet of fibers that underlies the epithelium, which lines the cavities and surfaces of organs including skin, or the endothelium, which lines the interior surface of blood vessels.- Composition :...

 in both the lung
Lung
The lung is the essential respiration organ in many air-breathing animals, including most tetrapods, a few fish and a few snails. In mammals and the more complex life forms, the two lungs are located near the backbone on either side of the heart...

 and the kidney
Kidney
The kidneys, organs with several functions, serve essential regulatory roles in most animals, including vertebrates and some invertebrates. They are essential in the urinary system and also serve homeostatic functions such as the regulation of electrolytes, maintenance of acid–base balance, and...

). The treatment of autoimmune diseases is typically with immunosuppression
Immunosuppression
Immunosuppression involves an act that reduces the activation or efficacy of the immune system. Some portions of the immune system itself have immuno-suppressive effects on other parts of the immune system, and immunosuppression may occur as an adverse reaction to treatment of other...

—medication which decreases the immune response.

Criteria

For a disease to be regarded as an autoimmune disease, it needs to answer to Witebsky's postulates (first formulated by Ernst Witebsky
Ernst Witebsky
Ernst Witebsky, also Ernest Witebsky was a German-American immunologist.From 1920 to 1926 Witebsky studied medicine at the University of Frankfurt and the University of Heidelberg. He stayed at Heidelberg after graduating and worked with Dr. Hans Sachs...

 and colleagues in 1957 and modified in 1994):
  • Direct evidence from transfer of pathogenic antibody or pathogenic T cells
  • Indirect evidence based on reproduction of the autoimmune disease in experimental animals, and
  • Circumstantial evidence from clinical clues

Classification

It is possible to classify autoimmune diseases by corresponding type of hypersensitivity
Hypersensitivity
Hypersensitivity refers to undesirable reactions produced by the normal immune system, including allergies and autoimmunity. These reactions may be damaging, uncomfortable, or occasionally fatal. Hypersensitivity reactions require a pre-sensitized state of the host. The four-group classification...

: type II
Type II hypersensitivity
In type II hypersensitivity the antibodies produced by the immune response bind to antigens on the patient's own cell surfaces...

, type III
Type III hypersensitivity
Type III hypersensitivity occurs when antigens and antibodies are present in roughly equal amounts, causing extensive cross-linking.-Presentation:...

, or type IV
Type IV hypersensitivity
Type IV hypersensitivity is often called delayed type hypersensitivity as the reaction takes two to three days to develop. Unlike the other types, it is not antibody mediated but rather is a type of cell-mediated response....

. (No type of autoimmune disease mimics type I hypersensitivity
Type I hypersensitivity
Type I hypersensitivity is an allergic reaction provoked by reexposure to a specific type of antigen referred to as an allergen, or to a nonimmunologic stimulus like cold weather or exercise...

.)

There is an on-going discussion about when a disease should be considered autoimmune, leading to different criteria such as Witebsky's postulates.
Name: Accepted/suspected Hypersensitivity
I, II, III, IV
Autoantibody >-
| Acute disseminated encephalomyelitis
Acute disseminated encephalomyelitis
Acute disseminated encephalomyelitis is an immune mediated disease of the brain. It usually occurs following a viral infection but may appear following vaccination, bacterial or parasitic infection, or even appear spontaneously. As it involves autoimmune demyelination, it is similar to multiple...

 (ADEM)
Accepted >-
| Addison's Disease
Addison's disease
Addison’s disease is a rare, chronic endocrine disorder in which the adrenal glands do not produce sufficient steroid hormones...

 
interferon omega; transglutaminase; aromatic acid carboxylase; GAD
Gad
Gad may refer to:In religion:*Gad , the founder of the tribe of Gad and seventh son of Jacob*Gad , King David's seer or prophet*Gad , a pan-Semitic deity worshipped during the Babylonian captivity...

; HAI
HAI
HAI may stand for:*List of IOC country codes for Haiti*Hellenic Aerospace Industry*Helicopter Association International*Hospital-acquired infection*Human Awareness Institute, an organization offering workshops on intimate relationships and sexuality...

; 17 hydroxylase; 21 hydroxylase 
>-
| Agammaglobulinemia 
IGHM
IGHM
Ig mu chain C region is a protein that in humans is encoded by the IGHM gene.It is associated with agammaglobulinemia-1.-Further reading:...

; IGLL1
IGLL1
Immunoglobulin lambda-like polypeptide 1 is a protein that in humans is encoded by the IGLL1 gene. IGLL1 has also recently been designated CD179B .It is associated with agammaglobulinemia-2.-Further reading:...

: CD79A
CD79A
CD79a molecule, immunoglobulin-associated alpha, also known as mb-1, is a human gene.The mb-1 gene codes for a phosphoprotein, designated CD79a CD79a molecule, immunoglobulin-associated alpha, also known as mb-1, is a human gene.The mb-1 gene codes for a phosphoprotein, designated CD79a CD79a...

; CD79B
CD79B
CD79b molecule, immunoglobulin-associated beta, also known as CD79B , is a human gene.It is associated with agammaglobulinemia-6.-External links:...

; BLNK; LRRC8A
LRRC8A
Leucine-rich repeat-containing protein 8A is a protein that in humans is encoded by the LRRC8A gene.It is associated with agammaglobulinemia-5.-Further reading:...


>-
| Alopecia areata
Alopecia areata
Alopecia areata is a medical condition in which hair is lost from some or all areas of the body, usually from the scalp. Because it causes bald spots on the scalp, especially in the first stages, it is sometimes called spot baldness. In 1–2% of cases, the condition can spread to the entire scalp ...

 
Accepted T-cells >-
| Amyotrophic Lateral Sclerosis
Amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis , also referred to as Lou Gehrig's disease, is a form of motor neuron disease caused by the degeneration of upper and lower neurons, located in the ventral horn of the spinal cord and the cortical neurons that provide their efferent input...

 
>-
| Ankylosing Spondylitis
Ankylosing spondylitis
Ankylosing spondylitis , previously known as Bekhterev's disease, Bekhterev syndrome, and Marie-Strümpell disease is a chronic inflammatory disease of the axial skeleton with variable involvement of peripheral joints and nonarticular structures...

 
Accepted ANCA
ANCA
ANCA Pty Ltd is an Australia company which designs and manufactures CNC grinding machines. The company was founded in 1974 by Pat Boland and Pat McCluskey in Melbourne, Australia....

?
CD8
CD8
CD8 is a transmembrane glycoprotein that serves as a co-receptor for the T cell receptor . Like the TCR, CD8 binds to a major histocompatibility complex molecule, but is specific for the class I MHC protein. There are two isoforms of the protein, alpha and beta, each encoded by a different gene...

; HLA-B27
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...


>-
| Antiphospholipid syndrome
Antiphospholipid syndrome
Antiphospholipid syndrome or antiphospholipid antibody syndrome , often also Hughes syndrome, is an autoimmune, hypercoagulable state caused by antibodies against cell-membrane phospholipids that provokes blood clots in both arteries and veins as well as pregnancy-related complications such as...

 
Accepted anti-cardiolipin;anti pyruvate dehydrogenase; β2 glycoprotein I; phosphatidylserine
Phosphatidylserine
Phosphatidylserine is a phospholipid component, usually kept on the inner-leaflet of cell membranes by an enzyme called flippase...

; anti apoH; Annexin A5
Annexin A5
Annexin A5 is a cellular protein in the annexin group. The function of the protein is unknown; however, annexin A5 has been proposed to play a role in the inhibition of blood coagulation by competing for phosphatidylserine binding sites with prothrombin and also to inhibit the activity of...

 
HLA-DR7
HLA-DR7
HLA-DR7 is a HLA-DR serotype that recognizes the DRB1*0701 to *0705 gene products.-Serology:The serological reaction of DR7 is excellent for *0701. The serology of *0703 to *0705 to *0709, and *0711 to *0714 serotypes is unknown. DRB1*0710N is a null allele. DRB1*0702 nomenclature has been...

, HLA-B8
HLA-B8
HLA-B8 is an HLA-B serotype. The serotype identifies the HLA-B*08 gene products. HLA-B8, previously known as HL-A8 was one of the first identified of the HLA antigens. It coined the "Super B8" haplotype, also called the ancestral European haplotype because of its common occurrence in Europe,...

, HLA-DR2
HLA-DR2
HLA-DR2 of the HLA-DR serotype system, is a broad antigen serotype that is now preferentially covered by HLA-DR15 and HLA-DR16 serotype group...

, HLA-DR3
HLA-DR3
HLA-DR3 is composed to the HLA-DR17 and HLA-DR18 split 'antigens' serotypes. DR3 is a component gene-allele of the AH8.1 haplotype in Northern and Western Europeans. Genes between B8 and DR3 on this haplotype are frequently associated with autoimmune disease....


>-
| Antisynthetase syndrome 
>-
| Atopic allergy 
I >-
| Atopic dermatitis
Atopic dermatitis
Atopic dermatitis is an inflammatory, chronically relapsing, non-contagious and pruritic skin disorder...

 
I >-
| Autoimmune aplastic anemia
Aplastic anemia
Aplastic anemia is a condition where bone marrow does not produce sufficient new cells to replenish blood cells. The condition, per its name, involves both aplasia and anemia...

 
>-
| Autoimmune cardiomyopathy 
Accepted >-
| Autoimmune enteropathy 
>-
| Autoimmune hemolytic anemia
Autoimmune hemolytic anemia
Autoimmune hemolytic anemia occurs when antibodies directed against the person's own red blood cells cause the RBCs to burst , leading to insufficient plasma concentration. The lifetime of the RBCs is reduced from the normal 100–120 days to just a few days in serious cases...

 
Accepted II >-
| Autoimmune hepatitis
Autoimmune hepatitis
Autoimmune Hepatitis is a disease of the liver that occurs when the body's immune system attacks cells of the liver. Anomalous presentation of human leukocyte antigen class II on the surface of hepatocytes, possibly due to genetic predisposition or acute liver infection, causes a cell-mediated...

 
Accepted cell-mediated anti-mitochondrial antibodies
Anti-mitochondrial antibodies
Anti-mitochondrial antibodies are autoantibodies, consisting of immunoglobulins formed against mitochondria, primarily mitochondria in cells of the liver...

; ANA
ANA
-Abbreviations:* AB Nyköpings Automobilfabrik* Administration for Native Americans, a program in the Administration for Children and Families* Afghan National Army* Agency for New Americans, a refugee organization in Boise, Idaho...

; anti-smooth muscle antibodies, LKM-1; soluble liver antigen
>-
| Autoimmune inner ear disease
Autoimmune inner ear disease
Autoimmune inner ear disease is a suspected autoimmune disease characterized by rapidly progressive bilateral sensorineural hearing loss. It occurs when the body's immune system attacks cells in the inner ear that are mistaken for a virus or bacteria. Autoimmune inner ear disease was first...

 
Accepted >-
| Autoimmune lymphoproliferative syndrome
Autoimmune lymphoproliferative syndrome
Autoimmune lymphoproliferative syndrome is a form of lymphoproliferative disorder. It affects lymphocyte apoptosis. It is a RASopathy.-Introduction:...

 
Accepted >-
| Autoimmune peripheral neuropathy 
Accepted >-
| Autoimmune pancreatitis
Autoimmune pancreatitis
Autoimmune pancreatitis is an increasingly recognized type of chronic pancreatitis that can be difficult to distinguish from pancreatic carcinoma but which responds to treatment with corticosteroids, particularly prednisone...

 
Accepted ANA
ANA
-Abbreviations:* AB Nyköpings Automobilfabrik* Administration for Native Americans, a program in the Administration for Children and Families* Afghan National Army* Agency for New Americans, a refugee organization in Boise, Idaho...

; anti-lactoferrin antibodiesanti-carbonic anhydrase antibodies; rheumatoid factor
Rheumatoid factor
Rheumatoid factor is an autoantibody most relevant in rheumatoid arthritis. It is defined as an antibody against the Fc portion of IgG. RF and IgG join to form immune complexes that contribute to the disease process...

>-
| Autoimmune polyendocrine syndrome
Autoimmune polyendocrine syndrome
In medicine, autoimmune polyendocrine syndromes are a heterogeneous group of rare diseases characterised by autoimmune activity against more than one endocrine organs, although non-endocrine organs can be affected....

 
Accepted Unknown or multiple Addison's Disease
Addison's disease
Addison’s disease is a rare, chronic endocrine disorder in which the adrenal glands do not produce sufficient steroid hormones...


>-
| Autoimmune progesterone dermatitis
Autoimmune progesterone dermatitis
Autoimmune progesterone dermatitis may appear as urticarial papules, deep gyrate lesions, papulovesicular lesions, an eczematous eruption, or as targetoid lesions. Autoimmune progesterone dermatitis initially manifests with eye symptoms, e.g. burning, and progresses into rashes...

 
Accepted >-
| Autoimmune thrombocytopenic purpura 
Accepted anti gpIIb-IIIa or 1b-IX >-
| Autoimmune urticaria 
Accepted >-
| Autoimmune uveitis 
Accepted HLAB-27? >-
| Balo disease/Balo concentric sclerosis
Balo concentric sclerosis
Balo concentric sclerosis is one of the borderline forms of multiple sclerosis.Balo concentric sclerosis is a demyelinating disease similar to standard multiple sclerosis, but with the particularity that the demyelinated tissues form concentric layers...

 
>-
| Bechets Syndrome 
>-
| Berger's disease 
IgA (elevated in 50% of patients), IgA (in mesangial deposits on kidney biopsy) >-
| Bickerstaff's encephalitis
Bickerstaff's encephalitis
Bickerstaff's encephalitis is a rare inflammatory disorder of the central nervous system, first described by Edwin Bickerstaff in 1951. It may also affect the peripheral nervous system, and has features in common with both Miller Fisher syndrome and Guillain-Barré syndrome.-Signs and symptoms:In...

 
Anti-GQ1b 2/3 patients Guillain-Barré syndrome
Guillain-Barré syndrome
Guillain–Barré syndrome , sometimes called Landry's paralysis, is an acute inflammatory demyelinating polyneuropathy , a disorder affecting the peripheral nervous system. Ascending paralysis, weakness beginning in the feet and hands and migrating towards the trunk, is the most typical symptom...


>-
| Blau syndrome
Blau syndrome
Blau syndrome is characterized by familial granulomatous arthritis, iritis, and skin granulomas, comprising an autosomal dominantly inherited syndrome that overlaps both sarcoidosis and granuloma annulare....

 
sarcoidosis
Sarcoidosis
Sarcoidosis , also called sarcoid, Besnier-Boeck disease or Besnier-Boeck-Schaumann disease, is a disease in which abnormal collections of chronic inflammatory cells form as nodules in multiple organs. The cause of sarcoidosis is unknown...

 and granuloma annulare
Granuloma annulare
Granuloma annulare is a chronic skin disease consisting of a rash with reddish bumps arranged in a circle or ring. Granuloma annulare is different from warts, and cryotherapy treatment will not work...


>-
| Bullous pemphigoid
Bullous pemphigoid
Bullous pemphigoid, also referred to as BP, is an acute or chronic autoimmune skin disease, involving the formation of blisters, more appropriately known as bullae, at the space between the skin layers epidermis and dermis.-Signs and symptoms:...

 
IgG autoantibodies targeting the type XVII collagen component of hemidesmosomes >-
| Cancer
Cancer
Cancer , known medically as a malignant neoplasm, is a large group of different diseases, all involving unregulated cell growth. In cancer, cells divide and grow uncontrollably, forming malignant tumors, and invade nearby parts of the body. The cancer may also spread to more distant parts of the...

 
>-
| Castleman's disease
Castleman's disease
Castleman's disease is an uncommon lymphoproliferative disorder that can involve single lymph node stations or...

 
>-
| Celiac disease 
Accepted IV?? Anti-tissue transglutaminase antibodies  HLA-DQ8
HLA-DQ8
HLA-DQ8 is a human leukocyte antigen serotype within the HLA-DQ serotype group. DQ8 is a split antigen of the DQ3 broad antigen. DQ8 is determined by the antibody recognition of β8 and this generally detects the gene product of DQB1*0302....

 and DQ2.5
>-
| Chagas disease
Chagas disease
Chagas disease is a tropical parasitic disease caused by the flagellate protozoan Trypanosoma cruzi. T. cruzi is commonly transmitted to humans and other mammals by an insect vector, the blood-sucking insects of the subfamily Triatominae most commonly species belonging to the Triatoma, Rhodnius,...

 
Suspected >-
| Chronic inflammatory demyelinating polyneuropathy
Chronic inflammatory demyelinating polyneuropathy
Chronic inflammatory demyelinating polyneuropathy is an acquired immune-mediated inflammatory disorder of the peripheral nervous system. The disorder is sometimes called chronic relapsing polyneuropathy. CIDP is closely related to Guillain-Barré syndrome and it is considered the chronic...

 
Anti-ganglioside antibodies
Anti-ganglioside antibodies
Anti-ganglioside antibodies that react to self-gangliosides are found in autoimmune neuropathies. These antibodies were first found to react with cerebellar cells...

:anti-GM1, anti-GD1a, anti-GQ1b
Guillain-Barré syndrome
Guillain-Barré syndrome
Guillain–Barré syndrome , sometimes called Landry's paralysis, is an acute inflammatory demyelinating polyneuropathy , a disorder affecting the peripheral nervous system. Ascending paralysis, weakness beginning in the feet and hands and migrating towards the trunk, is the most typical symptom...


>-
| Chronic recurrent multifocal osteomyelitis
Chronic recurrent multifocal osteomyelitis
Chronic recurrent multifocal osteomyelitis is also known as Chronic recurring multifocal osteomyelitis.-CRMO :Chronic recurrent multifocal osteomyelitis is a rare condition , in which the bones have lesions, inflammation, and pain. Its definition is evolving...

 
Majeed syndrome
Majeed syndrome
Majeed syndrome is an inherited skin disorder characterized by chronic multifocal osteomyelitis, congenital dyserythropoietic anemia and a neutrophilic dermatosis....


>-
| Chronic obstructive pulmonary disease
Chronic obstructive pulmonary disease
Chronic obstructive pulmonary disease , also known as chronic obstructive lung disease , chronic obstructive airway disease , chronic airflow limitation and chronic obstructive respiratory disease , is the co-occurrence of chronic bronchitis and emphysema, a pair of commonly co-existing diseases...

 
Suspected >-
| Churg-Strauss syndrome
Churg-Strauss syndrome
Churg–Strauss syndrome is a medium and small vessel autoimmune vasculitis, leading to necrosis. It involves mainly the blood vessels of the lungs , gastrointestinal system, and peripheral nerves, but also affects the heart, skin and kidneys. It is a rare disease that is non-inheritable and...

 
p-ANCA
P-ANCA
p-ANCA, or Perinuclear Anti-Neutrophil Cytoplasmic Antibodies, show a perinuclear staining pattern.This pattern occurs because the vast majority of the antigens targeted by ANCAs are highly cationic at pH 7.00. During ethanol fixation, antigens which are more cationic migrate and localize around...

>-
| Cicatricial pemphigoid
Cicatricial pemphigoid
Cicatricial pemphigoid is a rare chronic autoimmune subepithelial blistering disease characterized by erosive skin lesions of the mucous membranes and skin that results in scarring of at least some sites of involvement.Cicatricial pemphigoid has been referred...

 
anti-BP-1, anti BP-2 C3
C3
-Biology:* C3 carbon fixation in plants* C3-convertase, an enzyme* Apolipoprotein C3, a human very low density lipoprotein* ATC code C03 Diuretics, a subgroup of the Anatomical Therapeutic Chemical Classification System...


>-
| Cogan syndrome
Cogan syndrome
Cogan syndrome is a rare disorder characterized by recurrent inflammation of the front of the eye and often fever, fatigue, and weight loss, episodes of dizziness, and hearing loss. It can lead to deafness or blindness if untreated. The classic form of the disease was first described by D.G...

 
>-
| Cold agglutinin disease 
Accepted II IgM
IGM
IGM as an acronym or abbreviation can refer to:* Immunoglobulin M , the primary antibody against A and B antigens on red blood cells* International Grandmaster, a chess ranking* intergalactic medium* Intragroup medium - see: Intracluster medium...

>-
| Complement component 2 deficiency 
>-
| Contact dermatitis
Contact dermatitis
Contact dermatitis is a term for a skin reaction resulting from exposure to allergens or irritants . Phototoxic dermatitis occurs when the allergen or irritant is activated by sunlight....

 
III >-
| Cranial arteritis 
>-
| CREST syndrome
CREST syndrome
The limited cutaneous form of systemic scleroderma is often referred to as CREST syndrome. "CREST" is an acronym for the five main features:* Calcinosis* Raynaud's syndrome* Esophageal dysmotility* Sclerodactyly* Telangiectasia...

 
Anti-centromere antibodies
Anti-centromere antibodies
Anti-centromere antibodies occur in auto immune disorders; frequently in limited systemic scleroderma, , and, occasionally are found in the diffuse form of scleroderma...

 Anti-nuclear antibodies
>-
| Crohns Disease (one of two types of idiopathic inflammatory bowel disease "IBD")
Accepted IV ATG16L1
ATG16L1
Autophagy-related protein 16-1 is a protein that in humans is encoded by the ATG16L1 gene.-Function:Autophagy is the major intracellular degradation system delivering cytoplasmic components to lysosomes, and it accounts for degradation of most long-lived proteins and some organelles...

; CARD15;XBP1
XBP1
X-box binding protein 1, also known as XBP1, is a protein which in humans is encoded by the XBP1 gene. The XBP1 gene is located on chromosome 22 while a closely related pseudogene has been identified and localized to chromosome 5...

;
>-
| Cushing's Syndrome
Cushing's syndrome
Cushing's syndrome is a hormone disorder caused by high levels of cortisol in the blood. This can be caused by taking glucocorticoid drugs, or by tumors that produce cortisol or adrenocorticotropic hormone or CRH...

 
cortisol binding globulin? >-
| Cutaneous leukocytoclastic angiitis 
>-
| Dego's disease 
>-
| Dercum's disease 
Suspected >-
| Dermatitis herpetiformis
Dermatitis herpetiformis
Dermatitis herpetiformis , or Duhring's disease,Freedberg, et al. . Fitzpatrick's Dermatology in General Medicine. . McGraw-Hill. ISBN 0-07-138076-0. is a chronic blistering skin condition, characterised by blisters filled with a watery fluid...

 
IgA
IGA
Iga or IGA may stand for:-Given name:* a female given name of Polish origin. The name originates from the female given name Jadwiga and stands for gia,or gina in the USA....

; anti-epidermal transglutaminase antibodies
Keratinocyte transglutaminase
Protein-glutamine gamma-glutamyltransferase K is an enzyme that in humans is encoded by the TGM1 gene.Keratinocyte transglutaminase is a transglutaminase enzyme.-Pathology:...

 
>-
| Dermatomyositis
Dermatomyositis
Dermatomyositis is a connective-tissue disease related to polymyositis and Bramaticosis that is characterized by inflammation of the muscles and the skin.- Causes :...

 
Accepted histidine-tRNA anti-signal recognition peptide Anti-Mi-2 Anti-Jo1. >-
| Diabetes mellitus type 1
Diabetes mellitus type 1
Diabetes mellitus type 1 is a form of diabetes mellitus that results from autoimmune destruction of insulin-producing beta cells of the pancreas. The subsequent lack of insulin leads to increased blood and urine glucose...

 
Accepted IV Glutamic acid decarboxylase antibodies (GADA), islet cell antibodies (ICA), and insulinoma-associated autoantibodies (IA-2), anti-insulin antibodies  >-
| Diffuse cutaneous systemic sclerosis 
anti-nuclear antibodies, anti-centromere and anti-scl70/anti-topoisomerase antibodies
Anti-topoisomerase antibodies
Anti-topoisomerase antibodies are autoantibodies directed against topoisomerase and found in several diseases, most importantly scleroderma. Diseases with ATA are autoimmune disease because they react with self-proteins...

COL1A2
COL1A2
Collagen alpha-2 chain is a protein that in humans is encoded by the COL1A2 gene.-External links:* -Further reading:...

 and TGF-β1
>-
| Dressler's syndrome
Dressler's syndrome
Dressler's syndrome is a secondary form of pericarditis that occurs in the setting of injury to the heart or the pericardium...

 
myocardial neo-antigens formed as a result of the MI >-
| Drug-induced lupus 
anti-histone  >-
| Discoid lupus erythematosus
Discoid lupus erythematosus
Discoid lupus erythematosus is an uncommon autoimmune disease of the basal cell layer of the skin. It occurs in humans and cats, more frequently occurring in dogs. It does not progress to systemic lupus erythematosus in dogs. SLE can also have skin symptoms, but it appears that the two are...

 
III
>-
| Eczema
Eczema
Eczema is a form of dermatitis, or inflammation of the epidermis . In England, an estimated 5.7 million or about one in every nine people have been diagnosed with the disease by a clinician at some point in their lives.The term eczema is broadly applied to a range of persistent skin conditions...

 
SPINK5
SPINK5
Lympho-epithelial Kazal-type-related inhibitor also known as serine protease inhibitor Kazal-type 5 is a protein that in humans is encoded by the SPINK5 gene.- Structure and function :...

, filaggrin
Filaggrin
Filaggrin is a filament-associated protein that binds to keratin fibers in epithelial cells.-Profilaggrin:Filaggrin monomers are tandemly clustered into a large, 350kDa protein precursor known as profilaggrin. In the epidermis, these structures are present in the keratohyalin granules in cells of...

., Brain-derived neurotrophic factor
Brain-derived neurotrophic factor
Brain-derived neurotrophic factor, also known as BDNF, is a protein that, in humans, is encoded by the BDNF gene. BDNF is a member of the "neurotrophin" family of growth factors, which are related to the canonical "Nerve Growth Factor", NGF...

 (BDNF) and Substance P
Substance P
In the field of neuroscience, substance P is a neuropeptide: an undecapeptide that functions as a neurotransmitter and as a neuromodulator. It belongs to the tachykinin neuropeptide family. Substance P and its closely related neuropeptide neurokinin A are produced from a polyprotein precursor...

.
>-
| Endometriosis
Endometriosis
Endometriosis is a gynecological medical condition in which cells from the lining of the uterus appear and flourish outside the uterine cavity, most commonly on the ovaries. The uterine cavity is lined by endometrial cells, which are under the influence of female hormones...

 
Suspected >-
| Enthesitis
Enthesitis
Enthesitis is inflammation of the entheses, the sites where tendons or ligaments insert into the bone. It is also called enthesopathy, or any pathologic condition involving the entheses. The entheses are any point of attachment of skeletal muscles to the bone, where recurring stress or...

-related arthritis
. MMP3
MMP3
Stromelysin-1 also known as matrix metalloproteinase-3 is an enzyme that in humans is encoded by the MMP3 gene. The MMP3 gene is part of a cluster of MMP genes which localize to chromosome 11q22.3.- Function :...

 TRLR2, TLR4, ERAP1
>-
| Eosinophilic fasciitis
Eosinophilic fasciitis
Eosinophilic fasciitis , also known as "Shulman's syndrome",is a form of fasciitis. It is distinguished from scleroderma primarily because the affected area is the fascia, not the dermis as in scleroderma...

 
Accepted >- Eosinophilic gastroenteritis
Eosinophilic gastroenteritis
Eosinophilic gastroenteritis is a rare and heterogeneous condition characterized by patchy or diffuse eosinophilic infiltration of gastrointestinal tissue, first described by Kaijser in 1937...

 
IgE
IGE
IGE was one of the largest services company buying and selling virtual currencies and accounts for MMORPG. During its peak time, it had offices in Los Angeles, China , and headquarters & customer service centre in Hong Kong. IGE was one of the main monopoly in virtual economy services, also known...

 
IL-3
IL-3
IL-3 may refer to:* Interleukin 3* Illinois' 3rd congressional district* Illinois Route 3...

, IL-5
IL-5
IL 5 or IL-5 may refer to:* Interleukin 5* Illinois' 5th congressional district* Illinois Route 5...

, GM-CSF, eotaxin
Eotaxin
Eotaxin may refer to:* CCL11 * CCL24 * CCL26...


>-
| Epidermolysis bullosa acquisita
Epidermolysis bullosa acquisita
Epidermolysis bullosa acquisita is a chronic subepidermal blistering disease associated with autoimmunity to type VII collagen within anchoring fibril structures that are located at the dermal-epidermal junction....

 
COL7A1
COL7A1
Collagen alpha-1 chain is a protein that in humans is encoded by the COL7A1 gene.- Function :This gene encodes the alpha chain of type VII collagen. The type VII collagen fibril, composed of three identical alpha collagen chains, is restricted to the basement zone beneath stratified squamous...


>-
| Erythema nodosum
Erythema nodosum
Erythema nodosum is an inflammation of the fat cells under the skin characterized by tender red nodules or lumps that are usually seen on both shins...

 
>-
| Erthroblastosis fetalis
II ABO, Rh, Kell antibodies >-
| Essential mixed cryoglobulinemia 
>-
| Evan's syndrome 
>-
| Fibrodysplasia ossificans progressiva
Fibrodysplasia ossificans progressiva
Fibrodysplasia ossificans progressiva , sometimes referred to as Stone Man Syndrome, is an extremely rare disease of the connective tissue. A mutation of the body's repair mechanism causes fibrous tissue to be ossified when damaged. In many cases, injuries can cause joints to become permanently...

 
ACVR1
ACVR1
Activin A receptor, type I also known as ALK-2 is a protein which in humans is encoded by the ACVR1 gene.- Function :...

 Lymphocytes express increased BMP4
>-
| Fibrosing aveolitis aka Idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis is a chronic, progressive form of lung disease characterized by fibrosis of the supporting framework of the lungs...

 
SFTPA1
SFTPA1
Pulmonary surfactant-associated protein A1, also known as SFTPA1, is a human gene.-Further reading:...

, SFTPA2, TERT, and TERC
TERC
TERC may refer to:*Telomerase RNA component, a human gene.*The developers of the Investigations in Numbers, Data, and Space mathematics curriculum.*Technical Education Research Centers*CSIRO Tropical Ecosystems Research Centre...

.
>-
| Gastritis
Gastritis
Gastritis is an inflammation of the lining of the stomach, and has many possible causes. The main acute causes are excessive alcohol consumption or prolonged use of nonsteroidal anti-inflammatory drugs such as aspirin or ibuprofen. Sometimes gastritis develops after major surgery, traumatic...

 
serum antiparietal and anti-IF antibodies >-
| Gastrointestinal pemphigoid 
Accepted >-
| Giant cell arteritis 
>-
| Glomerulonephritis
Glomerulonephritis
Glomerulonephritis, also known as glomerular nephritis, abbreviated GN, is a renal disease characterized by inflammation of the glomeruli, or small blood vessels in the kidneys...

 
Sometimes IgA
IGA
Iga or IGA may stand for:-Given name:* a female given name of Polish origin. The name originates from the female given name Jadwiga and stands for gia,or gina in the USA....

 
Buerger's Disease
Buerger's disease
Thromboangiitis obliterans is a recurring progressive inflammation and thrombosis of small and medium arteries and veins of the hands and feet...

 for IgA
IGA
Iga or IGA may stand for:-Given name:* a female given name of Polish origin. The name originates from the female given name Jadwiga and stands for gia,or gina in the USA....

; Membranous glomerulonephritis
Membranous glomerulonephritis
Membranous glomerulonephritis is a slowly progressive disease of the kidney affecting mostly patients between ages of 30 and 50 years, usually Caucasian.It is one of the more common forms of nephrotic syndrome.-Terminology:...

 for IgG; Membranoproliferative/mesangiocapillary GN (Complement
Complement
In many different fields, the complement of X is something that together with X makes a complete whole—something that supplies what X lacks.Complement may refer to:...

 activation); Goodpasture's syndrome
Goodpasture's syndrome
Goodpasture’s syndrome is a rare disease characterized by glomerulonephritis and hemorrhaging of the lungs...

; Wegener's granulomatosis
Wegener's granulomatosis
Wegener's granulomatosis , more recently granulomatosis with polyangiitis , is an incurable form of vasculitis that affects the nose, lungs, kidneys and other organs. Due to its end-organ damage, it is life-threatening and requires long-term immunosuppression...


>-
| Goodpasture's syndrome
Goodpasture's syndrome
Goodpasture’s syndrome is a rare disease characterized by glomerulonephritis and hemorrhaging of the lungs...

 
Accepted II Anti-Basement Membrane Collagen Type IV Protein  >-
| Graves' disease
Graves' disease
Graves' disease is an autoimmune disease where the thyroid is overactive, producing an excessive amount of thyroid hormones...

 
Accepted II thyroid autoantibodies (TSHR-Ab) that activate the TSH
Thyroid-stimulating hormone
Thyrotrophin-stimulating hormone is a peptide hormone synthesized and secreted by thyrotrope cells in the anterior pituitary gland, which regulates the endocrine function of the thyroid gland.- Physiology :...

-receptor (TSHR)
>-
| Guillain-Barré syndrome
Guillain-Barré syndrome
Guillain–Barré syndrome , sometimes called Landry's paralysis, is an acute inflammatory demyelinating polyneuropathy , a disorder affecting the peripheral nervous system. Ascending paralysis, weakness beginning in the feet and hands and migrating towards the trunk, is the most typical symptom...

 (GBS)
Accepted IV Anti-ganglioside
Anti-ganglioside antibodies
Anti-ganglioside antibodies that react to self-gangliosides are found in autoimmune neuropathies. These antibodies were first found to react with cerebellar cells...

 
>-
| Hashimoto's encephalopathy
Hashimoto's encephalopathy
Hashimoto's Encephalopathy is a very rare condition associated with Hashimoto's thyroiditis. It was first described in 1966. It is classified as a neuroendocrine disorder....

 
Accepted IV alpha-enolase
Alpha-enolase
Enolase 1, more commonly known as alpha-enolase, is a glycolytic enzyme expressed in most tissues, one of the isozymes of enolase. It is a homodimer composed of 2 alpha subunits.-Relationship to Myc-binding protein-1:...

 
>-
| Hashimoto's thyroiditis
Hashimoto's thyroiditis
Hashimoto's thyroiditis or chronic lymphocytic thyroiditis is an autoimmune disease in which the thyroid gland is gradually destroyed by a variety of cell- and antibody-mediated immune processes. It was the first disease to be recognized as an autoimmune disease...

 
Accepted IV antibodies
Antibody
An antibody, also known as an immunoglobulin, is a large Y-shaped protein used by the immune system to identify and neutralize foreign objects such as bacteria and viruses. The antibody recognizes a unique part of the foreign target, termed an antigen...

 against thyroid peroxidase
Thyroid peroxidase
Thyroid peroxidase or thyroperoxidase is an enzyme expressed mainly in the thyroid that liberates iodine for addition onto tyrosine residues on thyroglobulin for the production of thyroxine or triiodothyronine , thyroid hormones. In humans, thyroperoxidase is encoded by the TPO...

 and/or thyroglobulin
Thyroglobulin
Thyroglobulin is a 660 kDa, dimeric protein produced by and used entirely within the thyroid gland. In earlier literature, Tg was referred to as colloid....

 
CTLA-4
CTLA-4
CTLA4 also known as CD152 is a protein that plays an important regulatory role in the immune system...


>-
| Henoch-Schonlein purpura
Henoch-Schönlein purpura
Henoch–Schönlein purpura is a disease of the skin and other organs that most commonly affects children. In the skin, the disease causes palpable purpura ; often with joint and abdominal pain...

 
immunoglobulin A (IgA) and complement component 3 (C3) >-
| Herpes gestationis aka Gestational Pemphigoid
Gestational pemphigoid
Gestational Pemphigoid or Pemphigoid Gestationis is a dermatosis of pregnancy, being an autoimmune blistering skin disease that occurs during pregnancy, typically in the second or third trimester, and/or immediately following pregnancy...

IgG and C3
C3
-Biology:* C3 carbon fixation in plants* C3-convertase, an enzyme* Apolipoprotein C3, a human very low density lipoprotein* ATC code C03 Diuretics, a subgroup of the Anatomical Therapeutic Chemical Classification System...

 misdirected antibodies intended to protect the placenta
>-
| Hidradenitis suppurativa
Hidradenitis suppurativa
Hidradenitis suppurativa is a skin disease that most commonly affects areas bearing apocrine sweat glands or sebaceous glands, such as the underarms, breasts, inner thighs, groin and buttocks.-Overview:...

 
Suspected >-
| Hypogammaglobulinemia
Hypogammaglobulinemia
Hypogammaglobulinemia is a type of immune disorder characterized by a reduction in all types of gamma globulins.Hypogammaglobulinemia is a characteristic of common variable immunodeficiency.-Terminology:...

 
IGHM
IGHM
Ig mu chain C region is a protein that in humans is encoded by the IGHM gene.It is associated with agammaglobulinemia-1.-Further reading:...

, IGLL1
IGLL1
Immunoglobulin lambda-like polypeptide 1 is a protein that in humans is encoded by the IGLL1 gene. IGLL1 has also recently been designated CD179B .It is associated with agammaglobulinemia-2.-Further reading:...

, CD79A
CD79A
CD79a molecule, immunoglobulin-associated alpha, also known as mb-1, is a human gene.The mb-1 gene codes for a phosphoprotein, designated CD79a CD79a molecule, immunoglobulin-associated alpha, also known as mb-1, is a human gene.The mb-1 gene codes for a phosphoprotein, designated CD79a CD79a...

, BLNK, LRRC8A
LRRC8A
Leucine-rich repeat-containing protein 8A is a protein that in humans is encoded by the LRRC8A gene.It is associated with agammaglobulinemia-5.-Further reading:...

, CD79B
CD79B
CD79b molecule, immunoglobulin-associated beta, also known as CD79B , is a human gene.It is associated with agammaglobulinemia-6.-External links:...


>-
| Idiopathic Inflammatory Demyelinating Diseases
Idiopathic inflammatory demyelinating diseases
Idiopathic inflammatory demyelinating diseases , sometimes known as borderline forms of multiple sclerosis, is a collection of multiple sclerosis variants, sometimes considered different diseases, but considered by others to form a spectrum differing only in terms of chronicity, severity, and...

 
multiple sclerosis
Multiple sclerosis
Multiple sclerosis is an inflammatory disease in which the fatty myelin sheaths around the axons of the brain and spinal cord are damaged, leading to demyelination and scarring as well as a broad spectrum of signs and symptoms...


>-
| Idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis is a chronic, progressive form of lung disease characterized by fibrosis of the supporting framework of the lungs...

 
SFTPA1
SFTPA1
Pulmonary surfactant-associated protein A1, also known as SFTPA1, is a human gene.-Further reading:...

, SFTPA2, TERT, and TERC
TERC
TERC may refer to:*Telomerase RNA component, a human gene.*The developers of the Investigations in Numbers, Data, and Space mathematics curriculum.*Technical Education Research Centers*CSIRO Tropical Ecosystems Research Centre...

.
>-
| Idiopathic thrombocytopenic purpura
Idiopathic thrombocytopenic purpura
Idiopathic thrombocytopenic purpura is the condition of having an abnormally low platelet count of no known cause . As most incidents of ITP appear to be related to the production of antibodies against platelets, immune thrombocytopenic purpura or immune thrombocytopenia are terms also used to...

 (See Autoimmune thrombocytopenic purpura)
Accepted II glycoprotein
Glycoprotein
Glycoproteins are proteins that contain oligosaccharide chains covalently attached to polypeptide side-chains. The carbohydrate is attached to the protein in a cotranslational or posttranslational modification. This process is known as glycosylation. In proteins that have segments extending...

s IIb-IIIa or Ib-IX, immunoglobulin G
Immunoglobulin G
Immunoglobulin G are antibody molecules. Each IgG is composed of four peptide chains — two heavy chains γ and two light chains. Each IgG has two antigen binding sites. Other immunoglobulins may be described in terms of polymers with the IgG structure considered the monomer.IgG constitutes 75%...


>-
| IgA nephropathy
IgA nephropathy
IgA nephropathy is a form of glomerulonephritis...

 
III? IgA
IGA
Iga or IGA may stand for:-Given name:* a female given name of Polish origin. The name originates from the female given name Jadwiga and stands for gia,or gina in the USA....

 produced from marrow rather than MALT
Malt
Malt is germinated cereal grains that have been dried in a process known as "malting". The grains are made to germinate by soaking in water, and are then halted from germinating further by drying with hot air...

 
>-
| Inclusion body myositis
Inclusion body myositis
Inclusion body myositis is an inflammatory muscle disease, characterized by slowly progressive weakness and wasting of both distal and proximal muscles, most apparent in the muscles of the arms and legs...

 
polymyositis
Polymyositis
Polymyositis is a type of chronic inflammation of the muscles related to dermatomyositis and inclusion body myositis.-Signs and symptoms:...

 but does not respond to steroid therapy-activated T8 cells
>-
| Chronic Inflammatory demyelinating polyneuropathy
Chronic inflammatory demyelinating polyneuropathy
Chronic inflammatory demyelinating polyneuropathy is an acquired immune-mediated inflammatory disorder of the peripheral nervous system. The disorder is sometimes called chronic relapsing polyneuropathy. CIDP is closely related to Guillain-Barré syndrome and it is considered the chronic...

 
anti-ganglioside antibodies
Anti-ganglioside antibodies
Anti-ganglioside antibodies that react to self-gangliosides are found in autoimmune neuropathies. These antibodies were first found to react with cerebellar cells...

>-
| Interstitial cystitis
Interstitial cystitis
Interstitial cystitis or bladder pain syndrome is a chronic, oftentimes severely debilitating disease of the urinary bladder...

 
Suspected >-
| Juvenile idiopathic arthritis
Juvenile idiopathic arthritis
Juvenile idiopathic arthritis is the most common form of persistent arthritis in children. JIA is a subset of arthritis seen in childhood, which may be transient and...

 aka Juvenile rheumatoid arthritis 
inconsistent ANA
ANA
-Abbreviations:* AB Nyköpings Automobilfabrik* Administration for Native Americans, a program in the Administration for Children and Families* Afghan National Army* Agency for New Americans, a refugee organization in Boise, Idaho...

 Rheumatoid factor
Rheumatoid factor
Rheumatoid factor is an autoantibody most relevant in rheumatoid arthritis. It is defined as an antibody against the Fc portion of IgG. RF and IgG join to form immune complexes that contribute to the disease process...

 
>-
| Kawasaki's Disease 
Suspected ITPKC
ITPKC
ITPKC is a gene that has been associated with Kawasaki disease.It codes an enzyme that negatively regulates T-cell activation....

 HLA-B51
HLA-B51
HLA-B51 is an HLA-B serotype. The serotype identifies the more common HLA-B*51 gene products.B51 is a split antigen of the broad antigen B5, and is a sister serotype of B52. There are a large number of alleles within the B*51 allele group...


>-
| Lambert-Eaton myasthenic syndrome
Lambert-Eaton myasthenic syndrome
Lambert–Eaton myasthenic syndrome is a rare autoimmune disorder that is characterised by muscle weakness of the limbs...

 
voltage-gated calcium channels; Q-type calcium channel
Q-type calcium channel
The Q-type calcium channel is a type of voltage-dependent calcium channel. Like the others of this class, the α1 subunit is the one that determines most of the channel's properties....

, synaptogagmin, muscarinic acetylcholine receptor M1
Muscarinic acetylcholine receptor M1
The muscarinic acetylcholine receptor M1, also known as the cholinergic receptor, muscarinic 1, is a muscarinic receptor.This receptor is found mediating slow EPSP at the ganglion in the postganglionic nerve, is common in exocrine glands and in the CNS.It is predominantly found bound to G proteins...

 
>-
| Leukocytoclastic vasculitis 
>-
| Lichen planus
Lichen planus
Lichen planus is a chronic mucocutaneous disease that affects the skin, tongue, and oral mucosa. The disease presents itself in the form of papules, lesions, or rashes. Lichen planus does not involve lichens, the fungus/algae symbionts that often grow on tree trunks; the name refers to the dry and...

 
>-
| Lichen sclerosus
Lichen sclerosus
Lichen sclerosus is an uncommon disease of unknown cause that results in white patches on the skin, which may cause scarring on and around genital skin....

 
>-
| Linear IgA disease (LAD)
>-
| Lou Gehrig's disease (Also Amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis , also referred to as Lou Gehrig's disease, is a form of motor neuron disease caused by the degeneration of upper and lower neurons, located in the ventral horn of the spinal cord and the cortical neurons that provide their efferent input...

)
VCP
VCP
VCP, a three-letter abbreviation with multiple meanings, including:In geography:*Van Cortlandt Park, New York City.In organizations:*Verband Christlicher Pfadfinderinnen und Pfadfinder, a German Scouting Association....

, ATXN2
ATXN2
Ataxin-2 is a protein that in humans is encoded by the ATXN2 gene.-Further reading:-External Links:*...

, OPTN, FIG4
Fig4
Polyphosphoinositide phosphatase also known as phosphatidylinositol 3,5-bisphosphate 5-phosphatase or SAC domain-containing protein 3 is an enzyme that in humans is encoded by the FIG4 gene.- Function :...

, TARDBP
TARDBP
TAR DNA-binding protein 43 , is a cellular protein which in humans is encoded by the TARDBP gene.- Discovery :TARDBP was originally identified as a transcriptional repressor that binds to chromosomally integrated TAR DNA and represses HIV-1 transcription. It was also reported to regulate alternate...

, ANG
ANG
ANG is the ISO 639-3 code for Old English. It may also refer to:* Air National Guard, part of the United States National Guard* Anga, Ang Desh or Ang Mahajanapada, one of the 16 Mahajanapada of Ancient India...

, VAPB
VAPB
Vesicle-associated membrane protein-associated protein B/C is a protein that in humans is encoded by the VAPB gene.-Further reading:...

, FUS
FUS
RNA-binding protein FUS is a protein that in humans is encoded by the FUS gene.- Function :The N-terminal end of FUS appears to be involved in transcriptional activation, while the C-terminal end is involved in protein and RNA binding...

, SETX
SETX
Probable helicase senataxin is an enzyme that in humans is encoded by the SETX gene.-External links:** -Further reading:http://ghr.nlm.nih.gov/gene/SETX...

, ALS2
ALS2
Alsin is a protein that in humans is encoded by the ALS2 gene. ALS2 orthologs have been identified in all mammals for which complete genome data are available.-External Links:** *...

, SOD1
SOD1
Superoxide dismutase [Cu-Zn] also known as superoxide dismutase 1 or SOD1 is an enzyme that in humans is encoded by the SOD1 gene. SOD1 is one of three human superoxide dismutases.- Function :...


>-
| Lupoid hepatitis
Lupoid hepatitis
Lupoid hepatitis is an auto-immune disease which causes liver cirrhosis. It maybe associated with systemic lupus erythematosus or other connective tissue disorders. 60% of patients have chronic hepatitis that may mimic viral hepatitis, but without serologic evidence of a viral infection...

 aka Autoimmune hepatitis
Autoimmune hepatitis
Autoimmune Hepatitis is a disease of the liver that occurs when the body's immune system attacks cells of the liver. Anomalous presentation of human leukocyte antigen class II on the surface of hepatocytes, possibly due to genetic predisposition or acute liver infection, causes a cell-mediated...

 
ANA and SMA, LKM-1 , LKM-2 or LKM-3; antibodies against soluble liver antigen(anti-SLA, anti-LP) no autoantibodies detected (~20%) >-
| Lupus erythematosus
Lupus erythematosus
Lupus erythematosus is a category for a collection of diseases with similar underlying problems with immunity . Symptoms of these diseases can affect many different body systems, including joints, skin, kidneys, blood cells, heart, and lungs...

 
Accepted III Anti-nuclear antibodies
Anti-nuclear antibody
Anti-nuclear antibodies are autoantibodies directed against contents of the cell nucleus....

 anti-Ro]]. Also, they are often present in Sjögren's syndrome
Sjögren's syndrome
Sjögren's syndrome , also known as "Mikulicz disease" and "Sicca syndrome", is a systemic autoimmune disease in which immune cells attack and destroy the exocrine glands that produce tears and saliva....

.
>-
| Majeed syndrome
Majeed syndrome
Majeed syndrome is an inherited skin disorder characterized by chronic multifocal osteomyelitis, congenital dyserythropoietic anemia and a neutrophilic dermatosis....

 
>-
| Ménière's disease
Ménière's disease
Ménière's disease is a disorder of the inner ear that can affect hearing and balance to a varying degree. It is characterized by episodes of vertigo and tinnitus and progressive hearing loss, usually in one ear. It is named after the French physician Prosper Ménière, who, in an article published...

 
III? major peripheral myelin protein P0 >-
| Microscopic polyangiitis
Microscopic polyangiitis
Microscopic polyangiitis is an ill-defined autoimmune disease characterized by pauci-immune, necrotizing, small-vessel vasculitis without clinical or pathological evidence of necrotizing granulomatous inflammation.-Presentation:Because many different organ systems may be involved, a wide range of...

 
p-ANCA
P-ANCA
p-ANCA, or Perinuclear Anti-Neutrophil Cytoplasmic Antibodies, show a perinuclear staining pattern.This pattern occurs because the vast majority of the antigens targeted by ANCAs are highly cationic at pH 7.00. During ethanol fixation, antigens which are more cationic migrate and localize around...

 myeloperoxidase
>-
| Miller-Fisher syndrome see Guillain-Barre Syndrome
Guillain-Barré syndrome
Guillain–Barré syndrome , sometimes called Landry's paralysis, is an acute inflammatory demyelinating polyneuropathy , a disorder affecting the peripheral nervous system. Ascending paralysis, weakness beginning in the feet and hands and migrating towards the trunk, is the most typical symptom...

Accepted >-
| Mixed Connective Tissue Disease
Mixed connective tissue disease
In medicine, mixed connective tissue disease , commonly abbreviated as MCTD, is an autoimmune disease, in which the body's defense system attacks itself. It was characterized in 1972....

 
Accepted anti-nuclear antibody
Anti-nuclear antibody
Anti-nuclear antibodies are autoantibodies directed against contents of the cell nucleus....

 anti-U1-RNP 
HLA-DR4
HLA-DR4
HLA-DR4 is a HLA-DR serotype that recognizes the DRB1*04 gene products. The DR4 serogroup is large and has a number ofmoderate frequency alleles spread over large regions of the world.-Serology:The serological identification of DR4 is good...


>-
| Morphea
Morphea
Morphea is a medical term for localized scleroderma. The disease involves isolated patches of hardened skin - there generally is no internal organ involvement.-Background, nomenclature, classification & codification :...

 
Suspected >-
| Mucha-Habermann disease aka Pityriasis lichenoides et varioliformis acuta
Pityriasis lichenoides et varioliformis acuta
Pityriasis lichenoides et varioliformis acuta is a disease of the immune system. It is the more severe version of Pityriasis lichenoides chronica...

>-
| Multiple sclerosis
Multiple sclerosis
Multiple sclerosis is an inflammatory disease in which the fatty myelin sheaths around the axons of the brain and spinal cord are damaged, leading to demyelination and scarring as well as a broad spectrum of signs and symptoms...

 
Suspected IV >-
| Myasthenia gravis
Myasthenia gravis
Myasthenia gravis is an autoimmune neuromuscular disease leading to fluctuating muscle weakness and fatiguability...

 
Accepted II nicotinic acetylcholine receptor
Nicotinic acetylcholine receptor
Nicotinic acetylcholine receptors, or nAChRs, are cholinergic receptors that form ligand-gated ion channels in the plasma membranes of certain neurons and on the postsynaptic side of the neuromuscular junction...

 MuSK protein
MuSK protein
MuSK is a receptor tyrosine kinase required for the formation of the neuromuscular junction. It is activated by a nerve-derived proteoglycan called agrin.-MuSK is required for formation of the Neuromuscular Junction:...

HLA-DR3
HLA-DR3
HLA-DR3 is composed to the HLA-DR17 and HLA-DR18 split 'antigens' serotypes. DR3 is a component gene-allele of the AH8.1 haplotype in Northern and Western Europeans. Genes between B8 and DR3 on this haplotype are frequently associated with autoimmune disease....

 HLA-DR1
HLA-DR1
HLA-DR1 is a HLA-DR serotype that recognizes the DRB1*01 gene products.-Serology:The serology for the most popular DR1 alleles is excellent. The serology for alleles , , , , , , and is unknown.-By serotype:...


>-
| Myositis
Myositis
Myositis is a general term for inflammation of the muscles. Many such conditions are considered likely to be caused by autoimmune conditions, rather than directly due to infection It is also a documented side effect of the lipid-lowering drugs statins and fibrates.Elevation of creatine kinase in...

 
Dermatomyositis
Dermatomyositis
Dermatomyositis is a connective-tissue disease related to polymyositis and Bramaticosis that is characterized by inflammation of the muscles and the skin.- Causes :...

 and Polymyositis
Polymyositis
Polymyositis is a type of chronic inflammation of the muscles related to dermatomyositis and inclusion body myositis.-Signs and symptoms:...

 see Inclusion-body-myositis
>-
| Narcolepsy
Narcolepsy
Narcolepsy is a chronic sleep disorder, or dyssomnia, characterized by excessive sleepiness and sleep attacks at inappropriate times, such as while at work. People with narcolepsy often experience disturbed nocturnal sleep and an abnormal daytime sleep pattern, which often is confused with insomnia...

 
Suspected II? hypocretin or orexin
Orexin
Orexins, also called hypocretins, are the common names given to a pair of excitatory neuropeptide hormones that were simultaneously discovered by two groups of researchers in rat brains....

 
HLA-DQB1
HLA-DQB1
Major histocompatibility complex, class II, DQ beta 1, also known as HLA-DQB1, is a human gene and also denotes the genetic locus that contains this gene...

*0602
>-
| Neuromyelitis optica (Also Devic's Disease)
II? NMO-IgG aquaporin 4
Aquaporin 4
Aquaporin 4 also known as AQP4 is protein which in humans is encoded by the AQP4 gene. AQP4 belongs to the aquaporin family of integral membrane proteins that conduct water through the cell membrane.- Function :...

.
>-
| Neuromyotonia
Neuromyotonia
Neuromyotonia , also known as Isaacs' syndrome, is a form of peripheral nerve hyperexcitability that causes spontaneous muscular activity resulting from repetitive motor unit action potentials of peripheral origin.-Causes:...

 
Suspected II? voltage-gated potassium channel
Voltage-gated potassium channel
Voltage-gated potassium channels are transmembrane channels specific for potassium and sensitive to voltage changes in the cell's membrane potential. During action potentials, they play a crucial role in returning the depolarized cell to a resting state....

s.
>-
| Occular cicatricial pemphigoid 
II? BP-1, BP-2 >-
| Opsoclonus myoclonus syndrome
Opsoclonus myoclonus syndrome
Opsoclonus Myoclonus Syndrome is a rare neurological disorder of unknown causes which appears to be the result of an autoimmune process involving the nervous system. It is an extremely rare condition, affecting as few as 1 in 10,000,000 people per year. It affects 2 to 3% of children with...

 
Suspected IV? >-
| Ord thyroiditis 
>-
| Palindromic rheumatism
Palindromic rheumatism
Palindromic Rheumatism consists of sudden and rapidly developing attacks of arthritis. There is acute pain, redness, swelling, and disability of one or multiple joints. The interval between recurrent attacks is extremely variable and how long the attack lasts is also variable...

 
>-
| PANDAS (pediatric autoimmune neuropsychiatric disorders associated with streptococcus)
Suspected II? >-
| Paraneoplastic cerebellar degeneration
Paraneoplastic cerebellar degeneration
Paraneoplastic cerebellar degeneration is a paraneoplastic syndrome associated with lung, ovarian, breast, and other cancers.As is the case with other paraneoplastic syndromes, PCD is believed to be due to an autoimmune reaction targeted against components of the central nervous system...

 
IV? II? anti-Yo (anti-cdr-2 in purkinje fibers) anti-Hu, anti-Tr, antiglutamate receptor >-
| Paroxysmal nocturnal hemoglobinuria
Paroxysmal nocturnal hemoglobinuria
Paroxysmal nocturnal hemoglobinuria , sometimes referred to as Marchiafava-Micheli syndrome, is a rare, acquired, potentially life-threatening disease of the blood characterised by complement-induced intravascular hemolytic anemia , red urine and thrombosis...

 (PNH)
Sometimes(?) >-
| Parry Romberg syndrome 
ANA >-
| Parsonnage-Turner syndrome 
>-
| Pars planitis 
>-
| Pemphigus vulgaris
Pemphigus vulgaris
Pemphigus vulgaris is a chronic blistering skin disease with skin lesions that are rarely pruritic, but which are often painful.-Pathophysiology:...

 
Accepted II >-
| Pernicious anaemia 
Accepted II anti-parietal cell antibody >-
| Perivenous encephalomyelitis 
>-
| POEMS syndrome
POEMS syndrome
POEMS syndrome is a rare medical syndrome. It is defined as the combination of a plasma-cell proliferative disorder , polyneuropathy, and effects on many other organ systems. It begins in middle age – the average age at onset is 50 – and affects up to twice as many men as women...

 
interleukin 1β
IL1B
Interleukin-1 beta also known as catabolin, is a cytokine protein that in humans is encoded by the IL1B gene. IL-1β precursor is cleaved by caspase 1 . Cytosolic thiol protease cleaves the product to form mature IL-1β.- Function :Interleukin 1 was discovered by Gery in 1972...

, interleukin 6
Interleukin 6
Interleukin-6 is a protein that in humans is encoded by the IL6 gene.IL-6 is an interleukin that acts as both a pro-inflammatory and anti-inflammatory cytokine. It is secreted by T cells and macrophages to stimulate immune response, e.g. during infection and after trauma, especially burns or other...

 and TNFα. vascular endothelial growth factor
Vascular endothelial growth factor
Vascular endothelial growth factor is a signal protein produced by cells that stimulates vasculogenesis and angiogenesis. It is part of the system that restores the oxygen supply to tissues when blood circulation is inadequate....

 (VEGF), given the .
>-
| Polyarteritis nodosa
Polyarteritis nodosa
Polyarteritis nodosa is a vasculitis of medium & small-sized arteries, which become swollen and damaged from attack by rogue immune cells. Polyarteritis nodosa is also called Kussmaul disease or Kussmaul-Maier disease...

 
>-
| Polymyalgia rheumatica
Polymyalgia rheumatica
Polymyalgia rheumatica , abbreviated as PMR, is a syndrome with pain or stiffness, usually in the neck, shoulders, and hips. The pain can be very sudden, or can occur gradually over a period of time...

 
>-
| Polymyositis
Polymyositis
Polymyositis is a type of chronic inflammation of the muscles related to dermatomyositis and inclusion body myositis.-Signs and symptoms:...

 
Accepted IFN-gamma, IL-1, TNF-alpha >-
| Primary biliary cirrhosis
Primary biliary cirrhosis
Primary biliary cirrhosis, often abbreviated PBC, is an autoimmune disease of the liver marked by the slow progressive destruction of the small bile ducts within the liver. When these ducts are damaged, bile builds up in the liver and over time damages the tissue. This can lead to scarring,...

 
Accepted Anti-p62
Anti-p62 antibodies
Anti-p62 antibodies are found in a primary biliary cirrhosis. p62 is also more frequent in Stage IV primary biliary cirrhosis and is prognostic for severe disease. The autoantigen is the nucleoporin 62kDA protein....

, Anti-sp100
Anti-sp100 antibodies
Anti-sp100 antibodies are found in association with primary biliary cirrhosis. The autoimmune target of anti-sp100 is the sp100 nuclear antigen which was identified by its association with primary biliary cirrhosis...

, Anti-Mitochondrial(M2)Anti-Ro aka SSA. Also, they are often present in Sjögren's syndrome
Sjögren's syndrome
Sjögren's syndrome , also known as "Mikulicz disease" and "Sicca syndrome", is a systemic autoimmune disease in which immune cells attack and destroy the exocrine glands that produce tears and saliva....

.
>-
| Primary sclerosing cholangitis
Primary sclerosing cholangitis
Primary sclerosing cholangitis is a chronic liver disease caused by progressive inflammation and scarring of the bile ducts of the liver. The inflammation impedes the flow of bile to the gut, which can ultimately lead to liver cirrhosis, liver failure and liver cancer...

 
primary biliary cirrhosis
Primary biliary cirrhosis
Primary biliary cirrhosis, often abbreviated PBC, is an autoimmune disease of the liver marked by the slow progressive destruction of the small bile ducts within the liver. When these ducts are damaged, bile builds up in the liver and over time damages the tissue. This can lead to scarring,...

?
>-
| Progressive inflammatory neuropathy
Progressive inflammatory neuropathy
Progressive inflammatory neuropathy is a disease that was identified in a report, released on January 31, 2008, by the Centers for Disease Control and Prevention. The first known outbreak of this neuropathy was in southeastern Minnesota in the United States. The disease was reported among pig...

 
Suspected >-
| Psoriasis
Psoriasis
Psoriasis is an autoimmune disease that appears on the skin. It occurs when the immune system mistakes the skin cells as a pathogen, and sends out faulty signals that speed up the growth cycle of skin cells. Psoriasis is not contagious. However, psoriasis has been linked to an increased risk of...

 
Accepted IV? HLA-C
HLA-C
HLA-C belongs to the MHC class I heavy chain receptors. The C receptor is a heterodimer consisting of a HLA-C mature gene product and β2-microglobulin. The mature C chain is anchored in the membrane...

w6, IL-12b, IL-23b]], TNFalpha, nfKb
>-
| Psoriatic arthritis
Psoriatic arthritis
Psoriatic arthritis is a type of inflammatory arthritis that, according to the National Psoriasis Foundation, will develop in up to 30 percent of people who have the chronic skin condition psoriasis...

 
Accepted IV? >-
| Pyoderma gangrenosum
Pyoderma gangrenosum
Pyoderma gangrenosum is a disease that causes tissue to become necrotic, causing deep ulcers that usually occur on the legs. When they occur, they can lead to chronic wounds. Ulcers usually initially look like small bug bites or papules, and they progress to larger ulcers. Though the wounds...

 
>-
| Pure red cell aplasia 
>-
| Rasmussen's encephalitis
Rasmussen's encephalitis
Rasmussen's encephalitis, also known as chronic focal encephalitis , is a rare inflammatory neurological disorder, characterized by frequent and severe seizures, loss of motor skills and speech, hemiparesis , encephalitis , and dementia...

 
anti-NR2A antibodies >-
| Raynaud phenomenon 
Suspected >-
| Relapsing polychondritis 
Accepted >-
| Reiter's syndrome 
>-
| Restless leg syndrome 
Suspected >-
| Retroperitoneal fibrosis
Retroperitoneal fibrosis
Retroperitoneal fibrosis or Ormond's disease is a disease featuring the proliferation of fibrous tissue in the retroperitoneum, the compartment of the body containing the kidneys, aorta, renal tract and various other structures. It may present with lower back pain, renal failure, hypertension, deep...

 
>-
| Rheumatoid arthritis
Rheumatoid arthritis
Rheumatoid arthritis is a chronic, systemic inflammatory disorder that may affect many tissues and organs, but principally attacks synovial joints. The process produces an inflammatory response of the synovium secondary to hyperplasia of synovial cells, excess synovial fluid, and the development...

 
Accepted III Rheumatoid factor
Rheumatoid factor
Rheumatoid factor is an autoantibody most relevant in rheumatoid arthritis. It is defined as an antibody against the Fc portion of IgG. RF and IgG join to form immune complexes that contribute to the disease process...

 (anti-IgGFc), Anti-MCV , ACPAs(Vimentin
Vimentin
Vimentin is a type III intermediate filament protein that is expressed in mesenchymal cells. IF proteins are found in all metazoan cells as well as bacteria. IF, along with tubulin-based microtubules and actin-based microfilaments, comprise the cytoskeleton...

 
HLA-DR4
HLA-DR4
HLA-DR4 is a HLA-DR serotype that recognizes the DRB1*04 gene products. The DR4 serogroup is large and has a number ofmoderate frequency alleles spread over large regions of the world.-Serology:The serological identification of DR4 is good...

, PTPN22
PTPN22
Protein tyrosine phosphatase, non-receptor type 22 , also known as PTPN22, is a protein that in humans is encoded by the PTPN22 gene. Alternative splicing of this gene results in two transcript variants encoding distinct isoforms...

, depleted B cells, TNF alpha, IL-17
IL-17
IL-17 or IL 17 can refer to:* Interleukin 17* Illinois' 17th congressional district* Illinois Route 17...

, (also maybe IL-1, 6, and 15)
>-
| Rheumatic fever
Rheumatic fever
Rheumatic fever is an inflammatory disease that occurs following a Streptococcus pyogenes infection, such as strep throat or scarlet fever. Believed to be caused by antibody cross-reactivity that can involve the heart, joints, skin, and brain, the illness typically develops two to three weeks after...

 
II streptococcal M protein
M protein (Streptococcus)
M protein is a virulence factor that can be produced by certain species of Streptococcus.Viruses, parasites and bacteria are covered in protein and sugar molecules that help them gain entry into a host by counteracting the host's defences. One such molecule is the M protein produced by certain...

 cross reacts with human myosin
Myosin
Myosins comprise a family of ATP-dependent motor proteins and are best known for their role in muscle contraction and their involvement in a wide range of other eukaryotic motility processes. They are responsible for actin-based motility. The term was originally used to describe a group of similar...

, anti-DNase B, ASO 
>-
| Sarcoidosis
Sarcoidosis
Sarcoidosis , also called sarcoid, Besnier-Boeck disease or Besnier-Boeck-Schaumann disease, is a disease in which abnormal collections of chronic inflammatory cells form as nodules in multiple organs. The cause of sarcoidosis is unknown...

 
Suspected IV. BTNL2
BTNL2
Butyrophilin-like protein 2 is a protein that in humans is encoded by the BTNL2 gene.-Further reading:...

; HLA-B7
HLA-B7
HLA-B7 is an HLA-B serotype. The serotype identifies the more common HLA-B*07 gene products. B7, previously HL-A7, was one of the first 'HL-A' antigens recognized, largely because of the frequency of B*0702 in Northern and Western Europe and the United States...

-DR15
HLA-DR15
HLA-DR15 is a HLA-DR serotype that recognizes the DRB1*1501 to *1505 and *1507 gene products. DR15 is found at high levels from Ireland to Central Asia. frequencies...

; HLA DR3-DQ2
HLA DR3-DQ2
HLA DR3-DQ2 is double serotype that specifically recognizes cells from individuals who carry a multigene HLA DR, DQ haplotype.Certain HLA DR and DQ genes have known involvementin autoimmune diseases. DR3-DQ2, a multigene...

.

>-
| Schizophrenia
Schizophrenia
Schizophrenia is a mental disorder characterized by a disintegration of thought processes and of emotional responsiveness. It most commonly manifests itself as auditory hallucinations, paranoid or bizarre delusions, or disorganized speech and thinking, and it is accompanied by significant social...

 
Suspected >-
| Schmidt syndrome another form of APS
anti-21 hydroxylase, anti-17 hydroxylase >-
| Schnitzler syndrome
Schnitzler syndrome
Schnitzler syndrome is a rare disease characterised by chronic hives and periodic fever, bone pain and joint pain , weight loss, malaise, fatigue, swollen lymph glands and enlarged spleen and liver....

 
>-
| Scleritis
Scleritis
Scleritis is a serious inflammatory disease that affects the white outer coating of the eye, known as the sclera. The disease is often contracted through association with other diseases of the body, such as Wegener's granulomatosis or rheumatoid arthritis; it can also be attained through disorders...

 
>-
| Scleroderma
Scleroderma
Systemic sclerosis or systemic scleroderma is a systemic autoimmune disease or systemic connective tissue disease that is a subtype of scleroderma.-Skin symptoms:...

 
Suspected IV? Scl-70 Anti-topoisomerase
Anti-topoisomerase antibodies
Anti-topoisomerase antibodies are autoantibodies directed against topoisomerase and found in several diseases, most importantly scleroderma. Diseases with ATA are autoimmune disease because they react with self-proteins...

>-
| Serum Sickness
Serum sickness
Serum sickness in humans is a reaction to proteins in antiserum derived from an non-human animal source. It is a type of hypersensitivity, specifically immune complex hypersensitivity . The term serum sickness–like reaction is occasionally used to refer to similar illnesses that arise from the...

 
III >-
| Sjögren's syndrome
Sjögren's syndrome
Sjögren's syndrome , also known as "Mikulicz disease" and "Sicca syndrome", is a systemic autoimmune disease in which immune cells attack and destroy the exocrine glands that produce tears and saliva....

 
Accepted Anti-ro]]. Also, they are often present in Sjögren's syndrome
Sjögren's syndrome
Sjögren's syndrome , also known as "Mikulicz disease" and "Sicca syndrome", is a systemic autoimmune disease in which immune cells attack and destroy the exocrine glands that produce tears and saliva....

.
>-
| Spondyloarthropathy
Spondyloarthropathy
Spondyloarthropathy is any joint disease of the vertebral column. Spondyloarthropathy with inflammation is called spondylarthritis. In contrast, spondylopathy is a disease of the vertebra itself, but many conditions involve both spondylopathy and spondyloarthropathy...

 
HLA-B27
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...


>-
| Still's disease
Still's disease
Still's disease can refer to:* Juvenile idiopathic arthritis* Adult-onset Still's disease...

 see Juvenile Rheumatoid Arthritis 
ANA
ANA
-Abbreviations:* AB Nyköpings Automobilfabrik* Administration for Native Americans, a program in the Administration for Children and Families* Afghan National Army* Agency for New Americans, a refugee organization in Boise, Idaho...

 
macrophage migration inhibitory factor
Macrophage migration inhibitory factor
Macrophage migration inhibitory factor also known as glycosylation-inhibiting factor , L-dopachrome isomerase, or phenylpyruvate tautomerase is a protein that in humans is encoded by the MIF gene.- Structure :...


>-
| Stiff person syndrome
Stiff person syndrome
Stiff person syndrome is a rare neurologic disorder of unknown etiology characterized by progressive rigidity and stiffness, primarily of the axial musculature, that is superimposed by spasms, resulting in postural deformities...

 
Suspected glutamic acid decarboxylase (GAD), GLRA1
GLRA1
Glycine receptor subunit alpha-1 is a protein that in humans is encoded by the GLRA1 gene.-Further reading:...

 (glycine receptor
Glycine receptor
The glycine receptor, or GlyR, is the receptor for the amino acid neurotransmitter glycine. GlyR is an ionotropic receptor that produces its effects through chloride current...


>-
| Subacute bacterial endocarditis (SBE)
III ]] essential mixed cryoglobulinemia >-
| Susac's syndrome
Susac's syndrome
Susac's syndrome is a microangiopathy characterized by encephalopathy, branch retinal artery occlusions and hearing loss. It is caused by the immune system attacking healthy tissue, and can lead to mental disorders....

 
>-
| Sweet's syndrome 
>-
| Sydenham chorea see PANDAS 
>-
| Sympathetic ophthalmia
Sympathetic ophthalmia
Sympathetic ophthalmia is a granulomatous uveitis of both eyes following trauma to one eye. It can leave the patient completely blind. Symptoms may develop from days to several years after a penetrating eye injury. See also the reviews by Damico et al. , Chu and Foster , and Friedlaender et al...

 
ocular antigens following trauma >-
| Systemic lupus erythematosis see Lupus erythematosis
III >-
| Takayasu's arteritis
Takayasu's arteritis
Takayasu's arteritis is a form of large vessel granulomatous vasculitis with massive intimal fibrosis and vascular narrowing affecting often young or middle-aged women of Asian descent...

 
>-
| Temporal arteritis
Temporal arteritis
Giant-cell arteritis or Horton disease is an inflammatory disease of blood vessels most commonly involving large and medium arteries of the head...

 (also known as "giant cell arteritis")
Accepted IV >-
| Thrombocytopenia
Thrombocytopenia
Thrombocytopenia is a relative decrease of platelets in blood.A normal human platelet count ranges from 150,000 to 450,000 platelets per microliter of blood. These limits are determined by the 2.5th lower and upper percentile, so values outside this range do not necessarily indicate disease...

 
II glycoprotein
Glycoprotein
Glycoproteins are proteins that contain oligosaccharide chains covalently attached to polypeptide side-chains. The carbohydrate is attached to the protein in a cotranslational or posttranslational modification. This process is known as glycosylation. In proteins that have segments extending...

s IIb-IIIa or Ib-IX in ITP
ITP
ITP can refer to:*Idiopathic thrombocytopenic purpura , a bleeding disorder*Individual Thought Patterns, the fifth album by death metal band Death*Industria de Turbo Propulsores, a Spanish gas turbine manufacturer...

 anti-ADAMTS13 in TTP
TTP
TTP may refer to:* Tehrik-i-Taliban Pakistan , the main Taliban militant umbrella group in Pakistan* Tenderness to palpation, a medical diagnostic such as in Trochleitis...

. and HUS
HUS
HUS is a three-letter acronym that may refer to the following:*Sikorsky HUS, US Navy helicopter, see Sikorsky H-34*Hemolytic-uremic syndrome* See also Hus...

 anti-cardiolipin
Cardiolipin
Cardiolipin is an important component of the inner mitochondrial membrane, where it constitutes about 20% of the total lipid composition. The only other place that cardiolipin can be found is in the membranes of most bacteria. The name ‘cardiolipin’ is derived from the fact that it was first...

 (anti-cardiolipin antibodies
Anti-cardiolipin antibodies
Anti-cardiolipin antibodies are antibodies often directed against cardiolipin and found in several diseases including syphilis, antiphospholipid syndrome, livedoid vasculitis, vertebrobasilar insufficiency, Behçet's syndrome, idiopathic spontaneous abortion, and systemic lupus erythematosus. They...

) and β2 glycoprotein I
Apolipoprotein H
Apolipoprotein H , previously known as , is a multifunctional apolipoprotein. One of its functions is to bind cardiolipin. When bound the structure of cardiolipin and Apo-H both undergo large changes in structure...

 in Antiphospholipid syndrome
Antiphospholipid syndrome
Antiphospholipid syndrome or antiphospholipid antibody syndrome , often also Hughes syndrome, is an autoimmune, hypercoagulable state caused by antibodies against cell-membrane phospholipids that provokes blood clots in both arteries and veins as well as pregnancy-related complications such as...

 anti-HPA-1a, anti-HPA-5b, and others in NAIT
NAIT
NAIT stands for:*North American Islamic Trust, an organization in Plainfield, Indiana, that owns Islamic properties*Northern Alberta Institute of Technology*Neonatal alloimmune thrombocytopenia*National Association of Industrial Technology...

 

>-
| Tolosa-Hunt syndrome
Tolosa-Hunt syndrome
Tolosa-Hunt syndrome is a rare disorder characterized by severe and unilateral headaches with extraocular palsies, usually involving the third, fourth, fifth, and sixth cranial nerves, and pain around the sides and back of the eye, along with weakness and paralysis of certain eye muscles.In 2004,...

 
>-
| Transverse myelitis
Transverse myelitis
Transverse myelitis is a neurological disorder caused by an inflammatory process of the spinal cord, and can cause axonal demyelination. The name is derived from Greek referring to the "spinal cord", and the suffix -itis, which denotes inflammation...

 
Accepted >-
| Ulcerative colitis
Ulcerative colitis
Ulcerative colitis is a form of inflammatory bowel disease . Ulcerative colitis is a form of colitis, a disease of the colon , that includes characteristic ulcers, or open sores. The main symptom of active disease is usually constant diarrhea mixed with blood, of gradual onset...

 (one of two types of idiopathic inflammatory bowel disease "IBD")
Accepted IV >-
| Undifferentiated connective tissue disease different from Mixed connective tissue disease
Accepted anti-nuclear antibody
Anti-nuclear antibody
Anti-nuclear antibodies are autoantibodies directed against contents of the cell nucleus....

 
HLA-DR4
HLA-DR4
HLA-DR4 is a HLA-DR serotype that recognizes the DRB1*04 gene products. The DR4 serogroup is large and has a number ofmoderate frequency alleles spread over large regions of the world.-Serology:The serological identification of DR4 is good...


>-
| Undifferentiated spondyloarthropathy 
>-
| Urticarial vasculitis
Urticarial vasculitis
Urticarial vasculitis is a skin condition characterized by fixed urticarial lesions that appear histologically as a vasculitis.- Introduction :A rare autoimmune disease characterised by recurrent...

 
II? anti C1q antibodies >-
| Vasculitis
Vasculitis
Vasculitis refers to a heterogeneous group of disorders that are characterized by inflammatory destruction of blood vessels. Both arteries and veins are affected. Lymphangitis is sometimes considered a type of vasculitis...

 
Accepted III sometimes ANCA >-
| Vitiligo
Vitiligo
Vitiligo is a condition that causes depigmentation of sections of skin. It occurs when melanocytes, the cells responsible for skin pigmentation, die or are unable to function. The cause of vitiligo is unknown, but research suggests that it may arise from autoimmune, genetic, oxidative stress,...

 
Suspected >-
| Wegener's granulomatosis
Wegener's granulomatosis
Wegener's granulomatosis , more recently granulomatosis with polyangiitis , is an incurable form of vasculitis that affects the nose, lungs, kidneys and other organs. Due to its end-organ damage, it is life-threatening and requires long-term immunosuppression...

 
Accepted Anti-neutrophil cytoplasmic(cANCA)
Anti-neutrophil cytoplasmic antibody
Anti-neutrophil cytoplasmic antibodies are a group of autoantibodies, mainly of the IgG type, against antigens in the cytoplasm of neutrophil granulocytes and monocytes...

 

Development of therapies

In both autoimmune and inflammatory diseases the condition arises through aberrant reactions of the human adaptive or innate immune systems. In autoimmunity, the patient’s immune system is activated against the body's own proteins. In inflammatory diseases, it is the overreaction of the immune system, and its subsequent downstream signaling (TNF, IFN, etc.), which causes problems.

A substantial minority of the population suffers from these diseases, which are often chronic, debilitating, and life-threatening. There are more than eighty illnesses caused by autoimmunity. It has been estimated that autoimmune diseases are among the ten leading causes of death among women in all age groups up to 65 years.

External links

The source of this article is wikipedia, the free encyclopedia.  The text of this article is licensed under the GFDL.
 
x
OK