Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Bronchocentric granulomatosis |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Silo-fillers' disease |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Toxic inhalation injury (disorder) |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Berylliosis |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Pneumoconiosis (disorder) |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Pulmonary granuloma |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Tropical pulmonary eosinophilia |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Asthmatic pulmonary eosinophilia |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Pulmonary mucormycosis |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Chronic pulmonary blastomycosis (disorder) |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
A rare idiopathic interstitial pneumonia characterized by prominent subpleural and parenchymal fibroelastosis and pleural fibrosis, predominantly involving the upper lobes. Signs and symptoms include non-productive cough, dyspnea, and recurrent respiratory infections. Pneumothorax is a frequently reported complication. Pulmonary function test reveals a restrictive pattern and reduced diffusing capacity. Computed tomography shows pleural thickening with signs of fibrosis (traction bronchiectasis, architectural distortion, and loss of volume), and reticulation. |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Acute pulmonary African histoplasmosis |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Chronic pulmonary African histoplasmosis |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Diffuse interstitial pulmonary fibrosis |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Acute exacerbation of idiopathic pulmonary fibrosis (disorder) |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
A rare disease, manifesting with idiopathic pulmonary fibrosis, hepatic nodular regenerative hyperplasia leading to portal hypertension and thrombocytopenia due to bone marrow hypoplasia. The condition was associated with 100% mortality. |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Familial idiopathic pulmonary fibrosis (disorder) |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Pulmonary melioidosis (disorder) |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Primary pneumonic plague |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Tuberculosis of anal canal |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Inflammatory cloacogenic polyp |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
A rare disorder related to pregnancy with characteristics of placental inflammatory process with clusters of histiocytes and associated fibrin in intervillous spaces, resulting in adverse pregnancy outcomes including intrauterine growth restriction, preterm birth, and pregnancy loss. Higher grading according to the proportion of involved intervillous space has been associated with poorer outcomes. There is a significant risk of recurrence in subsequent pregnancies. |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Visceral gout |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
A rare cerebellar ataxia characterized by cerebellar inflammation caused by viral or bacterial infection-triggered, immune-mediated mechanisms. It mainly affects young children following an episode of usually viral infection (notably varicella), but sometimes also adults, mostly upon Epstein-Barr virus or mycoplasma infection. Affected individuals mainly present with acute-onset afebrile gait ataxia, meningeal signs, high intracranial pressure with or without extracerebellar manifestations (such as clouding of consciousness, seizures and altered mental status) or extracerebellar focal signs. Mild behavioral changes can also be present. Pleocytosis in cerebrospinal fluid is reported in the majority of the patients. |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|
Sialodochitis |
Is a |
True |
Inflammation of specific body organs |
Inferred relationship |
Some |
|