Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Orofacial granulomatosis of gingivae |
Is a |
True |
Granulomatosis (disorder) |
Inferred relationship |
Some |
|
Bronchocentric granulomatosis |
Is a |
True |
Granulomatosis (disorder) |
Inferred relationship |
Some |
|
Granulomatosis with polyangiitis of nose |
Is a |
True |
Granulomatosis (disorder) |
Inferred relationship |
Some |
|
Granulomatosis with polyangiitis of larynx |
Is a |
True |
Granulomatosis (disorder) |
Inferred relationship |
Some |
|
Intraspinal granuloma |
Is a |
True |
Granulomatosis (disorder) |
Inferred relationship |
Some |
|
Intracranial granuloma |
Is a |
True |
Granulomatosis (disorder) |
Inferred relationship |
Some |
|
Familial granulomatous inflammatory arthritis, dermatitis and uveitis (disorder) |
Is a |
False |
Granulomatosis (disorder) |
Inferred relationship |
Some |
|
Granulomatosis with polyangiitis of gingiva |
Is a |
True |
Granulomatosis (disorder) |
Inferred relationship |
Some |
|
A rare systemic inflammatory disease with characteristics of early onset granulomatous arthritis, uveitis and skin rash. There are familial and sporadic forms of the same disease. The disease is due to an inherited or de novo mutation in the NOD2 gene (16q12), responsible for alterations in the innate immune response, inflammation and cell death. |
Is a |
False |
Granulomatosis (disorder) |
Inferred relationship |
Some |
|
A rare granulomatous autoinflammatory syndrome characterized by infantile-onset, widespread, chronic, recurrent, progressive, lobular panniculitis associated with panuveitis, arthritis and severe systemic granulomatous inflammation. |
Is a |
True |
Granulomatosis (disorder) |
Inferred relationship |
Some |
|
A rare, genetic, non-severe combined immunodeficiency disease characterised by immunodeficiency (manifested by recurrent and/or severe bacterial and viral infections), destructive noninfectious granulomas involving skin, mucosa and internal organs, and various autoimmune manifestations (including cytopenias, vitiligo, psoriasis, myasthenia gravis, enteropathy). Immunophenotypically, T-cell and B-cell lymphopenia, hypogammaglobulinaemia, abnormal specific antibody production and impaired T-cell function are observed. |
Is a |
True |
Granulomatosis (disorder) |
Inferred relationship |
Some |
|
Lymphomatoid granulomatosis |
Is a |
False |
Granulomatosis (disorder) |
Inferred relationship |
Some |
|
Lymphomatoid granulomatosis of lung (disorder) |
Is a |
False |
Granulomatosis (disorder) |
Inferred relationship |
Some |
|