Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Autoimmune parathyroiditis |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune endocrine disease |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Neutropenia associated with autoimmune disease |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Henoch-Sch?nlein purpura |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune leukopenia |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
An autoimmune coagulation disorder characterized by isolated thrombocytopenia (a platelet count <100,000/microL), in the absence of any underlying disorder that may be associated with thrombocytopenia. |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune pancytopenia |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune hemolytic anemia |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Antiphospholipid syndrome |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune purpura (disorder) |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Eaton-Lambert syndrome |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Myasthenia gravis |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune skin disease |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune encephalitis |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
FH: Autoimmune disease |
Associated finding |
False |
Autoimmune disease |
Inferred relationship |
Some |
1 |
Autoimmune disease NOS |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune disorder of inner ear |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Polymyositis associated with autoimmune disease |
Associated with |
True |
Autoimmune disease |
Inferred relationship |
Some |
2 |
Autoimmune hemolytic anemia (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Neutropenia associated with autoimmune disease |
Due to |
True |
Autoimmune disease |
Inferred relationship |
Some |
2 |
Immunoglobulin A vasculitis |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Sjögren's syndrome |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Rheumatoid arthritis |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Lung disorder due to autoimmune disorder (disorder) |
Due to |
True |
Autoimmune disease |
Inferred relationship |
Some |
1 |
Macrophage activation syndrome (disorder) |
Associated with |
False |
Autoimmune disease |
Inferred relationship |
Some |
1 |
FH: Autoimmune disease |
Associated finding |
True |
Autoimmune disease |
Inferred relationship |
Some |
1 |
Family history of lupus erythematosus (situation) |
Associated finding |
False |
Autoimmune disease |
Inferred relationship |
Some |
2 |
Lupus erythematosus |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Systemic sclerosis |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
FH: Autoimmune disease |
Associated finding |
False |
Autoimmune disease |
Inferred relationship |
Some |
1 |
Antisynthetase syndrome (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Pediatric autoimmune neuropsychiatric disorder associated with streptococcal infection (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune inflammation of skeletal muscle (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Rheumatoid arthritis |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune pancreatitis (disorder) |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune neonatal thrombocytopenia |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune liver disease |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune vasculitis (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Insulin resistance - type B |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
An arteriopathy characterized by visual loss, progressive or episodic deafness, and abnormal fundoscopy. |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Xerostomia due to autoimmune disease (disorder) |
Due to |
True |
Autoimmune disease |
Inferred relationship |
Some |
1 |
Autoimmune pulmonary alveolar proteinosis (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune cholangitis (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
A rare form of idiopathic inflammatory myopathy characterized by acute or subacute, severe, symmetrical, proximal muscle weakness usually associated with muscle-specific antibodies (anti-HMGCR or anti-SRP). Histopathological characteristics include myocyte necrosis and regeneration without significant inflammation, and C5b-9 deposition on non-necrotic myofibers. |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Vogt-Koyanagi-Harada disease |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Dianzani autoimmune lymphoproliferative disease (DALD) is a very rare disorder characterized by autoimmunity, lymphadenopathy and/or splenomegaly. |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Celiac disease, epilepsy and cerebral calcification syndrome (CEC) is a rare disorder characterized by the combination of auto-immune intestinal disease, epileptic seizures and cerebral calcifications. |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune enteropathy |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune myopathy (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune bullous dermatosis (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune keratitis (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
A clinical disease characterized by elevated serum IgG4 concentration and tumefaction or tissue infiltration by IgG4-positive plasma cells. |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
RAS-associated autoimmune leukoproliferative disease (RALD) is a rare genetic disorder characterized by monocytosis, autoimmune cytopenias, lymphoproliferation, hepatosplenomegaly, and hypergammaglobulinemia. |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune retinopathy (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune connective tissue disorder |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
dermatite/urticaire auto-immune à la progestérone |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune neutropenia |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Deformity of right hand co-occurrent and due to rheumatoid arthritis (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Deformity of left hand co-occurrent and due to rheumatoid arthritis (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Deformity of right foot co-occurrent and due to rheumatoid arthritis |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Deformity of left foot co-occurrent and due to rheumatoid arthritis |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Photodermatitis co-occurrent and due to autoimmune disease (disorder) |
Due to |
True |
Autoimmune disease |
Inferred relationship |
Some |
1 |
Photodermatitis co-occurrent and due to autoimmune disease (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Satoyoshi syndrome is a rare, multisystemic autoimmune disease mainly characterized by intermittent painful muscle spasms, alopecia (totalis or universalis in most cases) and long-lasting diarrhea that could lead to malnutrition, growth retardation, and amenorrhea. Secondary bone deformities and various endocrine anomalies may also be associated. Antinuclear antibodies are reported in many cases. |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune sensorineural hearing loss (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
A rare juvenile idiopathic inflammatory myopathy characterized by the association of inflammatory myositis (manifesting with acral erythema, progressive weakness of the limbs, pain, general fatigue, moodiness or crankiness) with clinical and/or laboratory features of other autoimmune diseases (e.g. systemic lupus erythematosus, localized scleroderma, diabetes). Cardiac involvement has been reported in some patients. |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
A rare, mixed autoinflammatory and autoimmune syndrome disorder characterized by recurrent neutrophilic blistering skin lesions, arthralgia, ocular inflammation, inflammatory bowel disease, absence of autoantibodies, and mild immunodeficiency manifested by recurrent sinopulmonary infections and deficiency of circulating antibodies. Inflammatory phenotype is not provoked by cold temperatures. |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
A rare, genetic, systemic autoimmune disease characterized by failure to thrive, global developmental delay, distinctive craniofacial dysmorphism (relative macrocephaly, dolichocephaly, frontal bossing, orbital proptosis, flattened midface with a prominent occiput, low, posteriorly rotated ears, micrognathia), hepato- and/or splenomegaly, and multisystemic autoimmune disease involving the lungs, liver, gut and/or thyroid gland. |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Erythema multiforme |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Seropositive rheumatoid arthritis |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Seronegative rheumatoid arthritis |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Rheumatoid arthritis of joint of spine |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Rheumatoid arthritis of left wrist (disorder) |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Rheumatoid arthritis of right wrist (disorder) |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Rheumatoid arthritis of multiple joints (disorder) |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
A rare genetic cerebral small vessel disease characterized by progressive loss of visual acuity due to retinal vasculopathy, in combination with more variable neurological signs and symptoms including stroke, cognitive decline, migraine-like headaches, and seizures, among others, typically beginning in middle age. Psychiatric features such as depression and anxiety may also occur. Systemic vascular involvement with Raynaud phenomenon, micronodular liver cirrhosis, and glomerular kidney dysfunction is present in a subset of patients. |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Acute disseminated encephalomyelitis |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
A rare immune dysregulation disease with immunodeficiency characterized by severe, progressive infantile onset inflammatory bowel disease with pancolitis, perianal disease (ulceration, fistulae), recurrent respiratory, genitourinary and cutaneous infections, arthritis and a high risk of B-cell lymphoma. |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Guillain-Barré syndrome |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Anti-glomerular basement membrane disease (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune ganglionopathy |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune optic neuropathy (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune opsoclonus myoclonus |
Due to |
True |
Autoimmune disease |
Inferred relationship |
Some |
1 |
Autoimmune urticaria and/or angioedema (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Myocarditis due to autoimmune disease (disorder) |
Due to |
True |
Autoimmune disease |
Inferred relationship |
Some |
2 |
Chondrodysplasia punctata due to maternal autoimmune disease (disorder) |
Due to |
True |
Autoimmune disease |
Inferred relationship |
Some |
2 |
Herpes gestationis |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Rheumatic arthritis |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Rheumatic fever |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Recurrent rheumatic heart disease |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Chronic rheumatic pericarditis |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Chronic rheumatic carditis |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Pernicious anaemia due to autoimmune disorder |
Due to |
True |
Autoimmune disease |
Inferred relationship |
Some |
1 |
Macrophage activation syndrome due to juvenile systemic onset arthritis |
Associated with |
False |
Autoimmune disease |
Inferred relationship |
Some |
4 |
Rheumatoid factor negative and anti-citrullinated protein antibody negative juvenile polyarthritis |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Rheumatoid factor negative and anti-citrullinated protein antibody positive juvenile polyarthritis |
Is a |
False |
Autoimmune disease |
Inferred relationship |
Some |
|
Extra-articular rheumatoid process |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Juvenile idiopathic arthritis (disorder) |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
A rare genetic immune disease characterized by recurrent sinopulmonary infections and autoimmune enterocolopathy, manifesting as frequent episodes of intractable diarrhea with abdominal pain and fever, accompanied by eczematous rashes, due to deficits in components of innate and adaptive immunity. Immunologic abnormalities include IgG subclass deficiency, impaired antigen-induced lymphocyte proliferation, reduced cytokine production by CD8+ T lymphocytes, and decreased numbers of natural killer cells. |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
Autoimmune male infertility |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|
A rare, primary immunodeficiency characterized by variable combination of enteropathy, hypogammaglobulinemia, recurrent respiratory infections, granulomatous lymphocytic interstitial lung disease, lymphocytic infiltration of non-lymphoid organs (intestine, lung, brain, bone marrow, kidney), autoimmune thrombocytopenia or neutropenia, autoimmune hemolytic anemia and lymphadenopathy. |
Is a |
True |
Autoimmune disease |
Inferred relationship |
Some |
|