Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Immunoglobulin A vasculitis |
Is a |
True |
Autoimmune vasculitis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Systemic lupus erythematosus encephalitis |
Is a |
True |
Autoimmune vasculitis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Rheumatoid vasculitis |
Is a |
True |
Autoimmune vasculitis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Rheumatoid arteritis |
Is a |
False |
Autoimmune vasculitis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Allergic granulomatosis angiitis (disorder) |
Is a |
True |
Autoimmune vasculitis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
STING-associated vasculopathy with onset in infancy |
Is a |
True |
Autoimmune vasculitis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Microscopic polyangiitis (disorder) |
Is a |
True |
Autoimmune vasculitis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acute rheumatic fever with aortitis (disorder) |
Is a |
True |
Autoimmune vasculitis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Immunoglobulin G4 related aortitis (disorder) |
Is a |
True |
Autoimmune vasculitis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Vasculitis due to ADA2 deficiency is a rare, genetic, systemic and rheumatologic disease due to adenosine deaminase-2 inactivating mutations, combining variable features of autoinflammation, vasculitis, and a mild immunodeficiency. Variable clinical presentation includes chronic or recurrent systemic inflammation with fever, livedo reticularis or racemosa, early-onset ischemic or hemorrhagic strokes, peripheral neuropathy, abdominal pain, hepatosplenomegaly, portal hypertension, cutaneous polyarteritis nodosa, variable cytopenia and immunoglobulin deficiency. |
Is a |
True |
Autoimmune vasculitis (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|