Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Mild persistent asthma uncontrolled co-occurrent with allergic rhinitis (disorder) |
Is a |
True |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|
Moderate persistent asthma uncontrolled co-occurrent with allergic rhinitis (disorder) |
Is a |
True |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|
Adult onset Still's disease |
Is a |
True |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|
Schnitzler syndrome (disorder) |
Is a |
True |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|
Acute generalized pustular flare of preexisting plaque psoriasis (disorder) |
Is a |
True |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|
Cryptogenic pulmonary eosinophilia |
Is a |
True |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|
A rare, genetic, multisystemic, chronic autoimmune disease characterized by the presence of systemic lupus erythematosus symptoms in two or more members of a single family. Patients present a wide spectrum of clinical manifestations, including cutaneous (malar rash, photosensitivity), ocular (keratoconjunctivitis sicca, retinopathy), gastrointestinal (oral ulceration, abdominal pain), cardiac (atherosclerosis, chest pain), pulmonary (serositis, pleurisy), musculoskeletal (arthralgia, myalgia), renal (nephritis, hematuria), obstetrical (increased spontaneous abortions, neonatal lupus), constitutional (fatigue, loss of appetite) and neuropsychiatric (mood and cognitive disorders) involvement, among others. |
Is a |
True |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|
A rare non-severe combined immunodeficiency characterised by tumour necrosis factor-dependent chronic mucocutaneous ulcerations and inflammatory bowel disease presenting during the first years of life. Ulcerations occur primarily in the oral, gastrointestinal, and vaginal mucosa. |
Is a |
True |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|
PAPASH syndrome |
Is a |
False |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|
A rare autoinflammatory syndrome with characteristics of a chronic-relapsing course of the combination of pyoderma gangrenosum, acne, hidradenitis suppurativa (which, in addition to axillae and inguinal folds, can be observed on upper and lower limbs, back, and buttocks, among others), and ankylosing spondylitis. Typical age of onset is adolescence to young adulthood, with the different signs and symptoms appearing simultaneously or subsequently. |
Is a |
False |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|
A rare hyper-IgE syndrome with characteristics of atopic dermatitis (eczema), chronic mucocutaneous candidiasis, and elevated IgE levels due to ZNF341 deficiency. High plasma levels of IgG and low natural killer (NK) cell numbers are observed. Other major clinical features involve recurrent skin infections with skin abscesses and connective tissue abnormalities. Some patients may have recurrent lung infections. |
Is a |
True |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|
Multiple sclerosis |
Is a |
True |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|
Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to DIAPH1 mutation |
Is a |
True |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|
Lung disease, immunodeficiency, chromosome breakage syndrome (disorder) |
Is a |
True |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|
Cogan's syndrome (disorder) |
Is a |
True |
Chronic disease of immune function (disorder) |
Inferred relationship |
Some |
|