{
    "disease_id": "DOID:0050159", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009537", 
            "description": "Interstitial pneumonia characterized by the presence of bibasilar pulmonary interstitial infiltrates composed of lymphocytes and plasma cells. It may be associated with autoimmune and lymphoproliferative disorders. Signs and symptoms include fever, cough, and dyspnea. Symptomatic patients may require immunosuppressive treatment.", 
            "resource": "MONDO", 
            "id": "MONDO:0009537", 
            "name": "lymphoid interstitial pneumonia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009537", 
            "name": "lymphoid interstitial pneumonia; LIP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009537", 
            "name": "lymphocytic interst. pneumonitis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009537", 
            "name": "diffuse hyperplasia of bronchus-associated lymphoid tissue"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009537", 
            "name": "lymphoid interstitial pneumonia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009537", 
            "name": "lymphocytic interstitial pneumonitis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009537", 
            "name": "LIP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009537", 
            "name": "lymphocytic interstitial pneumonia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050159", 
        "description": "An idiopathic interstitial pneumonia which involves diffuse interstitial infiltration of involved areas mostly with T lymphocytes, plasma cells, and macrophages. Lymphoid hyperplasia is frequently seen. Onset is often slow with gradually increasing cough and breathlessness over 3 or more years. Fever, weight loss, chest pain, and arthralgia are occasionally found. Crackles may be detected as the disease progresses.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050159", 
        "name": "lymphoid interstitial pneumonia"
    }
}