Autoimmune and Autoinflammatory Diseases with Inflammatory Arthritis (AiArthritis Diseases)
There are over 100 autoimmune and autoinflammatory diseases, originating from different parts of the immune system. However, only a fraction of these diseases present inflammation-driven arthritis as a clinical symptom in most patients. These are the diseases we represent.
By focusing on these specific conditions, we can highlight their similarities and differences from other autoimmune/autoinflammatory diseases and types of arthritis. This approach can help raise global awareness and expedite the processes of detection, referrals, diagnosis, and treatment, ultimately resulting in a better quality of life and higher rates of remission for those affected.
The distinction between autoimmune and autoinflammatory diseases, or a combination of both, lies in where the disease was triggered in the immune system. Understanding these differences is crucial for proper diagnosis and management.

Learn more about the differences between autoimmune and autoinflammatory diseases to further understand the complexities of these conditions.
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Common Symptoms of AiArthritis Diseases
The following list of early disease features is derived from our comprehensive research into patient-reported symptoms of our core diseases. This research includes data from our Early Symptoms of AiArthritis study, publications by scientific societies and rheumatology clinics, and feedback from our patient organization partners. These symptoms were reported by at least 30% of all patients in the early stages of the disease, regardless of their core disease diagnosis. We define early disease as occurring within the first 12 months from onset.
Common In All AiArthritis Diseases
Common in All AiArthritis Diseases
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FlaresList Item 1
Flares: Periods of worsening symptoms are called flares. A flare can last for hours, days, weeks, or months.
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Physical ActivityList Item 2
Physical Activity: Condition improves with activity and exercise and worsens with rest.
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ComorbiditiesList Item 3
Comorbidities: When inflammation is left uncontrolled due to lack of proper treatment, comorbidities can develop. 70% of patients with chronic, lifelong disease will develop comorbidities, including dual or triple diagnoses.
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Family HistoryList Item 4
Family History: Autoimmune diseases often run in families, indicating a potential genetic predisposition where that gene can cause disease. Autoinflammatory diseases can occur multiple times in a family, but is based off of genetic mutation. It is not a gene that causes the disease— but a mutation on the gene that can cause the disease which can then be passed on to the next generation.
Autoimmune or Autoinflammatory Arthritis Disease Features
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FatigueList Item 1
Fatigue that is severe and unusual, not immediately corrected with rest or caffeine. ( > 95%)
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Flu-like symptomsList Item 2
Flu-like symptoms, without having the flu- nausea, muscle weakness, and general malaise. ( > 50%)
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Brain FogList Item 3
"Brain fog", or finding it difficult to put thoughts together. This symptom historically has been mostly associated with lupus, but it is common in the other core diseases. ( > 30%)
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FeverList Item 4
Fever, typically low grade in autoimmune (with exception of juvenile idiopathic arthritis) and higher grade in autoinflammatory (% strongly varies per core disease)
Inflammatory Arthritis Features of AiArthritis Diseases
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Joint PainList Item 1
Joint pain in at least one joint lasting for longer than six weeks and not due to injury, other condition, or medication. (Required for differentiating this type of arthritis from mechanical pain and osteoarthritis)
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StiffnessList Item 2
Severe stiffness, which is worse after rest or inactivity. Many patients report they suddenly feel like their bed is uncomfortable because of the severe stiffness after rest. ( > 50%)
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SwellingList Item 3
Redness and/or swelling around the joints ( > 30%)
Typically the joint pain will coincide with the autoimmune and autoinflammatory disease features and start and stop suddenly - for no apparent reason (which is called a "flare"). Some people will experience all of the above symptoms, others only a few. If you have any of the arthritis features, and at least one of the autoimmune/autoinflammatory features, please consult your physician about a referral to a specialist.
Reference: Early Symptoms of AiArthritis Study, AiArthritis, 2019. Discover more
AiArthritis Diseases that most overlap in presentation and symptoms
*Over the past few years, research has shown that spondyloarthritis may be a little bit of both autoimmune to autoinflammatory, as most diseases fall somewhere along a continuum.
AiArthritis is dedicated to keeping informed about this new information, including how it may impact other similar diseases.
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Rheumatoid Arthritis (RA)List Item 1
Rheumatoid arthritis (RA) is a chronic inflammatory condition that can affect your joints, tissues, and organs. RA is an autoimmune disease where the immune system mistakenly attacks healthy tissue.
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Psoriatic Arthritis (PsA)List Item 2
Psoriatic arthritis (PsA) is a chronic inflammatory disease. It affects the joints and often causes enthesitis (inflammation where tendons and ligaments attach to bones). PsA can also impact the skin and eyes. While most people with PsA have a psoriasis rash, it can be hidden (like on the scalp) or may not show up for years.
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Sjögren's Disease (SD)List Item 4
Sjögren’s disease affects your body’s moisture-producing glands, causing dryness in areas like your eyes, mouth, and skin. It can also affect organs like your lungs and kidneys.
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Systemic Lupus Erythematosus (SLE)List Item 3
Lupus is a disease where the immune system attacks healthy parts of your body, like joints, skin, and organs. It can be unpredictable, with periods where it gets worse (flares) and times when it gets better.
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Axial Spondyloarthritis (axSpA)
Axial Spondyloarthritis (axSpA) is a condition that mainly affects the spine and the area where your pelvis meets your spine. It can also affect organs like the eyes and intestines. There are two types:
- Non-radiographic axSpA: No visible damage on x-rays.
- Ankylosing Spondylitis (AS): Damage can be seen on x-rays.
*Over the past few years, research has shown that spondyloarthritis may be a little bit of both autoimmune to autoinflammatory, as most diseases fall somewhere along a continuum. AiArthritis is dedicated to keeping informed about this new information, including how it may impact other similar diseases.
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Still's Disease (SD)
Still’s Disease is a rare, multi-systemic (whole body) autoinflammatory condition that can vary from person to person. Because of a similar pathogenesis, broadly overlapping symptoms, and organ involvement, Still’s Disease represents a disease continuum that includes both Systemic Juvenile Idiopathic Arthritis (SJIA) and Adult-Onset Still’s Disease (AOSD).
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Juvenile Idiopathic Arthritis (JIA)List Item 3
JIA is a term used to define juvenile onset disease (younger than age 16) that affects children and adolescents. There are juvenile versions of almost of the diseases under our AiArthritis disease umbrella (i.e., lupus, sjogren's disease, etc.). What was once called juvenile rheumatoid arthritis in now referred to as Juvenile Idiopathic Arthritis (JIA), which involves many subgroups and is not specific to a juvenile version of rheumatoid arthritis.
JIA is the most common rheumatic disease in childhood. The term "idiopathic" means that the cause of the condition is unknown. Several subtypes fall under the JIA umbrella including:
Oligoarthritis: the most common subtype that affects four or fewer joints, typically including the knees, elbows, or ankles. Oligoarthritis can be further divided into:
- Persistent: Affecting a limited number of joints throughout the disease course
- Extended: Involving more joints after the initial presentation
Polyarthritis: Affects five or more joints, often both sides of the body.
Systemic: Involves the entire body with symptoms such as high fever, rash, and inflammation of internal organs. The fever is usually daily, and the rash may be evanescent, meaning it comes and goes. Systemic JIA can affect multiple joints and can have more systemic complications.
Undifferentiated: This category is used when the features of JIA do not fit into one specific subtype. It may include children who do not meet the criteria for any of the other subtypes or exhibit features of more than one subtype. Inflammation is present in one or more joints for at least 6 weeks.
Enthesitis-Related Arthritis: Enthesitis refers to inflammation where tendons or ligaments attach to bones. This subtype of JIA involves inflamed enthesitis and usually arthritis/joints, too - but not always. Enthesitis can occur often in various parts of the body, like the chest or feet. Subgroups ERA may evolve into:
- Juvenile Axial Spondyloarthritis: Specifically affecting the spine/lower back.
- Juvenile Psoriatic Arthritis: Characterized by both arthritis (and likely enthesitis) and psoriasis or a family history of psoriasis. Psoriasis is a skin condition that causes red, scaly patches.
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Undifferentiated Disease (UD)List Item 4
When autoimmune and autoinflammatory diseases with inflammation-driven arthritis as a major component are not fully developed, or overlap so that a precise diagnosis cannot be determined, they are often given an "undifferentiated" diagnosis.
See More Information Below
Additional AiArthritis Diseases that may have more differentiating symptoms
These diseases are also categorized under the AiArthritis umbrella; however, we have distinguished them to emphasize their unique features, which can more readily differentiate them from the conditions in the initial group.
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Crohn's DiseaseList Item 1
Crohn’s Disease is a chronic condition that causes inflammation in the digestive tract, especially in the small and large intestines. Crohn’s Disease is a type of Inflammatory Bowel Disease (IBD) and is often paired with Ulcerative Colitis as the most common types of IBD. Crohn’s Disease is under the AiArthritis umbrella with arthritic symptoms.
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SarcoidosisList Item 2
Sarcoidosis is an inflammatory disease characterized by the formation of sarcoid granulomas—tiny clumps of inflammatory cells—in one or more organs of the body. When the immune system goes into overdrive and too many of these clumps form, they can interfere with an organ’s structure and function. When left unchecked, chronic inflammation can lead to fibrosis, which is the permanent scarring of organ tissue. This disorder affects the lungs or lymph nodes in approximately 90% of cases, but it can affect almost any organ in the body.
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Relapsing Polychondritis (RP)List Item 3
Relapsing Polychondritis (RP) is a rare autoimmune disease that causes inflammation of cartilage in the body. It most commonly affects the ears, nose, airways, and joints but can also involve the eyes, heart, and brain.
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Mixed Connective Tissue Disease (MCTD)
MCTD is a rare autoimmune disorder where patients have features of more than one rheumatic disease, such as lupus, scleroderma, and polymyositis. It is identified by the presence of anti-U1-ribonucleoprotein (anti-RNP) antibodies in the blood.
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Systemic Sclerosis (SSc)
Systemic sclerosis (also called scleroderma) is a rare autoimmune disease that causes the skin to harden and can also affect organs like the lungs or heart. It happens when the immune system makes too much collagen, leading to inflammation and damage in the body.
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Behcet's Disease (BD)List Item 2
Behcet’s disease is a rare condition that causes inflammation of the blood vessels (vasculitis). It can affect various parts of the body, including the mouth, eyes, skin, and internal organs.
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Palindromic Rheumatism (PR) Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.List Item 3
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VEXAS Syndrome
VEXAS (Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic) syndrome is a rare autoinflammatory disorder that was first identified in 2020. This syndrome is characterized by a combination of symptoms, including recurrent fevers, blood abnormalities, and inflammatory skin lesions. The term "VEXAS" reflects some of the key features of the syndrome.
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Antisynthetase Syndrome (ASS)
Antisynthetase syndrome is a rare autoimmune disease that can affect different parts of the body. It is usually associated with antibodies (like Anti-Jo1) that attack proteins in the body. This condition is a type of myositis (muscle inflammation).
Very Rare AiArthritis Diseases
There are also some very rare autoinflammatory diseases that often include inflammatory arthritis as a major clinical component. These include:
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Familial Mediterranean Fever (FMF)List Item 1
Familial Mediterranean Fever (FMF) is a genetic disorder that causes repeated episodes of pain and inflammation in the abdomen, chest, joints, and skin, along with fever. It mostly affects people from Mediterranean backgrounds, such as Arab, Armenian, Turkish, and Sephardic Jewish populations. FMF comes in two types:
- FMF Type 1: Causes recurring inflammation and symptoms like fever, abdominal pain, chest pain, and joint pain. If not treated, it can lead to kidney problems due to a buildup of a protein called amyloidosis.
- FMF Type 2: The main symptom is amyloidosis, even if other FMF symptoms aren’t present.
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Hyper-Immunoglobin D Syndrome (HIDS)List Item 2
Hyper IgD Syndrome (HIDS), also called mevalonate kinase deficiency (MKD), is a rare autoinflammatory disease caused by a genetic mutation. This mutation affects the mevalonate kinase enzyme, leading to inflammation in the body. Symptoms usually begin in early childhood and happen in episodes, meaning they come and go with periods of little to no symptoms in between.
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Chronic Nonbacterial Osteomyelitis (CNO)List Item 3
Chronic Nonbacterial Osteomyelitis (CNO) also called Chronic Recurrent Multifocal Osteomyelitis (CRMO) is a rare autoinflammatory disease where the bones become inflamed without infection. It causes long-term bone pain and swelling, often affecting the long bones, pelvis, shoulder, and spine. The disease mostly occurs in children.
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Schnitzler SyndromeList Item 1
Schnitzler syndrome is a rare autoinflammatory disease. People with this condition usually have non-itchy hives (urticaria) and abnormal levels of certain proteins in their blood, especially a protein called monoclonal IgM gammopathy.
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Cryopyrin-Associated Periodic Syndromes (CAPS)List Item 2
Cryopyrin-Associated Periodic Syndromes (CAPS) are a group of rare genetic disorders characterized by recurrent episodes of inflammation and related symptoms. CAPS is caused by mutations in the NLRP3 gene, which provides instructions for making a protein called cryopyrin. Cryopyrin is involved in the regulation of the immune system, specifically in the process of inflammation.
There are three main conditions within the CAPS spectrum, which vary in terms of severity:
- Familial Cold Autoinflammatory Syndrome (FCAS): This is the mildest form of CAPS. Symptoms are triggered or worsened by exposure to cold temperatures. Patients experience rash, fever, joint pain, and other signs of inflammation during these episodes.
- Muckle-Wells Syndrome (MWS): MWS is a moderate form of CAPS. Symptoms are more persistent and may not always be triggered by cold exposure. Patients with MWS experience recurrent fever, rash, joint pain, and eye redness. Progressive hearing loss can also occur.
- Chronic Infantile Neurological, Cutaneous, and Articular Syndrome (CINCA) or Neonatal-Onset Multisystem Inflammatory Disease (NOMID): CINCA/NOMID is the most severe form of CAPS. Symptoms begin in infancy and include rash, joint swelling, chronic meningitis, and skeletal abnormalities. Neurological symptoms are also common, leading to developmental delays.
Other Autoimmune and Autoinflammatory Conditions
There are several types of arthritis beyond autoimmune, autoinflammatory, and degenerative forms, such as gout. Reactive Arthritis is not included in this list because it is often a reaction to an infection from another part of the body and is not necessarily immune-inspired. Fibromyalgia is excluded as it is a nerve condition, not an AiArthritis disease. Additionally, there are over 80 other types of autoimmune and autoinflammatory diseases that may involve arthritis, but it is typically not a major disease feature in most patients and not a diagnostic feature early in onset.
Associated Conditions
These are some conditions that often occur alongside our core diseases. In some cases, these conditions are natural extensions of the diseases mentioned above. For example, lupus nephritis is the progression of kidney disease in patients with Systemic Lupus Erythematosus. In several of our diseases, eye inflammation is a primary symptom, while in others, it is a comorbidity, a complication caused by uncontrolled inflammation.
The rationale behind our formation was to unite similar diseases that are either autoimmune or autoinflammatory, all presenting the same type of arthritis early in the disease. We believe this approach will help expedite detection, referrals, and diagnosis, leading to earlier intervention, higher remission rates, and better disease outcomes. If there is an autoimmune or autoinflammatory disease where arthritis is a core feature and present in most patients, but it is not on this list, please email info@aiarthritis.org with "Disease Addition" in the subject line. We review our disease list annually with a team of medical specialists and will update it as necessary.
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FibromyalgiaList Item 1
Fibromyalgia is a chronic condition characterized by widespread pain, fatigue, and tenderness in muscles, ligaments, and tendons. It frequently coexists with autoimmune and autoinflammatory arthritis, causing additional pain and fatigue, and is often misunderstood to be an autoimmune disease
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Heart DiseaseList Item 2
Heart disease encompasses a range of conditions affecting the heart, including coronary artery disease, heart attacks, and heart failure. Autoimmune and autoinflammatory arthritis can increase the risk of heart disease due to chronic inflammation.
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Interstitial Lung DiseaseList Item 3
Interstitial lung disease includes a group of lung disorders that cause scarring of lung tissue, leading to breathing difficulties and reduced oxygen intake. Inflammatory arthritis can cause lung inflammation and scarring, contributing to these lung issues.
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DysautonomiaList Item 4
Dysautonomia is a disorder of the autonomic nervous system, affecting heart rate, blood pressure, digestion, and temperature regulation. It often occurs in patients with autoimmune diseases, causing symptoms like lightheadedness and fatigue.
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Neuropathy/Peripheral
Neuropathy refers to damage to peripheral nerves causing pain, numbness, and weakness, usually in the hands and feet. It is common in autoimmune diseases due to nerve inflammation or damage from chronic disease.
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Raynaud's PhenomenonList Item 1
Raynaud's phenomenon is a condition where blood flow to fingers and toes is restricted, leading to cold, numb, and discolored extremities. It often occurs with autoimmune diseases like scleroderma and lupus, as inflammation affects blood vessels.
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Eye InflammationList Item 2
Eye inflammation includes conditions such as uveitis, iritis, scleritis, and ocular inflammation, causing pain, redness, and vision problems. It can be a complication of autoimmune and autoinflammatory arthritis.
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Dental IssuesList Item 3
Potential dental issues include gum inflammation, periodontal disease, and tooth decay. Inflammation from autoimmune diseases can affect oral health, leading to increased dental problems.
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VasculitisList Item 4
Vasculitis is the inflammation of blood vessels, causing reduced blood flow and potential damage to organs and tissues. It can occur with autoimmune diseases, leading to symptoms like rashes, fatigue, and organ damage.
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Myositis/Polymyositis/Dermatomyositis
Myositis, polymyositis, and dermatomyositis are conditions involving muscle inflammation, causing muscle weakness and pain. They are often associated with autoimmune diseases, leading to muscle inflammation and weakness
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Celiac's DiseaseList Item 1
Celiac disease is an autoimmune disorder where ingestion of gluten leads to damage in the small intestine. It frequently coexists with other autoimmune diseases, causing digestive issues and nutrient absorption problems.
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ThyroidismList Item 2
Thyroidism encompasses disorders of the thyroid gland, including hypothyroidism (underactive thyroid) and hyperthyroidism (overactive thyroid). Autoimmune thyroid diseases like Hashimoto's thyroiditis and Graves' disease are common in patients with other autoimmune conditions.
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Lupus NephritisList Item 3
Lupus nephritis is an inflammation of the kidneys caused by systemic lupus erythematosus (SLE), leading to kidney damage. It is a severe complication of lupus, affecting kidney function and health.
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IgG4List Item 4
IgG4-related disease (IgG4-RD) is a chronic inflammatory condition characterized by tissue infiltration with IgG4-positive plasma cells, causing tissue enlargement and organ dysfunction. It can coexist with autoimmune diseases, leading to inflammation in various organs.
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Osteoarthritis
Osteoarthritis is a degenerative joint disease causing cartilage breakdown, leading to pain, stiffness, and reduced mobility. Though not autoimmune, it is a rhuematic disease and it can coexist with inflammatory arthritis, exacerbating joint pain and disability.
References:
- Our Early Symptoms of AiArthritis Study
- Undifferentiated Connective-Tissue Disease, Hildebrand, B., et al; Medscape, 2018.
- https://www.rheumatology.org/I-Am-A/Patient-Caregiver/Diseases-Conditions/Spondyloarthritis