Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Multiple supernumerary teeth related to systemic condition |
Associated with |
True |
Systemic disease |
Inferred relationship |
Some |
2 |
Anaphylaxis |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|
Non-allergic anaphylaxis |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|
Extra-articular rheumatoid process |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|
Exfoliation of teeth due to systemic disease |
Due to |
True |
Systemic disease |
Inferred relationship |
Some |
2 |
Generalized precocious exfoliation of teeth due to systemic disease (disorder) |
Due to |
True |
Systemic disease |
Inferred relationship |
Some |
2 |
Inflammatory bowel disease is a systemic disorder comprised of two major disorders: ulcerative colitis and Crohn disease. Crohn disease can affect any part of the digestive system while ulcerative colitis is confined to the colon. Both disorders may affect sites outside of the digestive system. |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|
Male infertility due to systemic disease (disorder) |
Due to |
True |
Systemic disease |
Inferred relationship |
Some |
3 |
Hereditary paediatric Behçet-like disease |
Is a |
False |
Systemic disease |
Inferred relationship |
Some |
|
A rare systemic disease characterized by acute or subacute onset of thrombocytopenia, anasarca (edema, pleural effusion, ascites), and systemic inflammation (fever and/or elevated C-reactive protein). Minor diagnostic categories are Castleman's disease-like features on lymph node biopsy, reticulin myelofibrosis and/or increased number of megakaryocytes in bone marrow, progressive renal insufficiency, and mild organomegaly including hepatosplenomegaly and lymphadenopathy. Most patients show elevated levels of serum alkaline phosphatase, while marked polyclonal hypergammopathy is rare. |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|
A rare, genetic, lymphoproliferative syndrome characterized by early onset recurrent infections, lymphadenopathy with hepatosplenomegaly and variable autoimmune disorders, including hemolytic anemia, thrombocytopenia, neutropenia, enteropathy, type I diabetes, scleroderma, arthritis, atopic dermatitis, and inflammatory lung disease. Patients commonly have failure to thrive. Variable immunologic findings include decreased regulatory T-cells, hypogammaglobulinemia, and reduction in memory B cells. |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|
Acute pancreatitis due to systemic disease (disorder) |
Due to |
True |
Systemic disease |
Inferred relationship |
Some |
3 |
Dysmotility of small intestine due to systemic disease |
Due to |
True |
Systemic disease |
Inferred relationship |
Some |
3 |
Primary lymphoedema with systemic involvement |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|
A rare systemic condition affecting patients undergoing chimeric antigen receptor (CAR) T-cell therapy and characterized by a systemic inflammatory response due to massive activation of leukocytes with subsequent cytokine release. It can present with a variety of signs and symptoms ranging from mild, flu-like symptoms (such as fever, fatigue, headache, rash, arthralgia, and myalgia) to severe life-threatening manifestations including vascular leakage, disseminated intravascular coagulation, shock, and multiple organ failure. Respiratory manifestations are common and range from cough and tachypnea to acute respiratory distress syndrome (ARDS). |
Is a |
False |
Systemic disease |
Inferred relationship |
Some |
|
Immune effector cell-associated neurotoxicity syndrome (disorder) |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|
Retinitis pigmentosa due to systemic disease |
Due to |
True |
Systemic disease |
Inferred relationship |
Some |
2 |
Cytokine-associated toxicity (disorder) |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|
Vasculitis due to systemic disease |
Due to |
True |
Systemic disease |
Inferred relationship |
Some |
2 |
Secondary systemic vasculitis |
Is a |
False |
Systemic disease |
Inferred relationship |
Some |
|
Primary systemic vasculitis (disorder) |
Is a |
False |
Systemic disease |
Inferred relationship |
Some |
|
Primary systemic arteritis (disorder) |
Is a |
False |
Systemic disease |
Inferred relationship |
Some |
|
Polyarteritis |
Is a |
False |
Systemic disease |
Inferred relationship |
Some |
|
Ocular hypertension due to systemic syndrome |
Due to |
True |
Systemic disease |
Inferred relationship |
Some |
3 |
A rare autoinflammatory syndrome with characteristics of adult onset of rheumatologic manifestations such as recurrent fever, skin and pulmonary inflammation, ear and nose chondritis, vasculitis, deep vein thrombosis and arthralgia. Laboratory examination reveals progressive hematologic abnormalities including macrocytic anemia and thrombocytopenia, as well as elevated inflammatory markers. Bone marrow biopsy shows hypercellularity and signs of bone marrow dysplasia. The disease primarily occurs in males and is caused by somatic mutations on chromosome Xp11. |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|
Systemic onset juvenile chronic arthritis |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|
Haploinsufficiency of A20 |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|
Systemic onset juvenile idiopathic arthritis of knee (disorder) |
Is a |
False |
Systemic disease |
Inferred relationship |
Some |
|
Ocular hypertension of left eye due to systemic syndrome (disorder) |
Due to |
True |
Systemic disease |
Inferred relationship |
Some |
3 |
Ocular hypertension of right eye due to systemic syndrome (disorder) |
Due to |
True |
Systemic disease |
Inferred relationship |
Some |
3 |
Bilateral ocular hypertension due to systemic syndrome |
Due to |
True |
Systemic disease |
Inferred relationship |
Some |
5 |
Open angle glaucoma of left eye due to systemic syndrome (disorder) |
Due to |
True |
Systemic disease |
Inferred relationship |
Some |
2 |
Glaucoma of right eye due to systemic syndrome |
Due to |
True |
Systemic disease |
Inferred relationship |
Some |
2 |
Open angle glaucoma of bilateral eyes due to systemic syndrome (disorder) |
Due to |
True |
Systemic disease |
Inferred relationship |
Some |
3 |
A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease. |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|
Crohn's disease that affects parts of the body outside of the digestive system is known as extraintestinal Crohn's and is commonly related to the joints, skin, and eyes and organs like the kidney and liver. |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|
Systemic lupus erythematosus |
Is a |
True |
Systemic disease |
Inferred relationship |
Some |
|