{
    "disease_id": "DOID:0060941",
    "recommended_name": {
        "id": "DOID:0060941",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060941",
        "name": "interstitial lung disease 1",
        "description": "An interstitial lung disease characterized by a progressive remodeling of the alveolar interstitium that has_material_basis_in heterozygous mutation in the SFTPA1 gene on chromosome 10q22."
    },
    "synonyms": [
        {
            "id": "DOID:0060941",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060941",
            "name": "Idiopathic pulmonary fibrosis",
            "description": ""
        },
        {
            "id": "MONDO:0030608",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030608",
            "name": "interstitial lung disease 1",
            "description": "An interstitial lung disease in which the cause of the disease is a variation in the SFTPA1 gene."
        },
        {
            "id": "MONDO:0030608",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030608",
            "name": "ILD1",
            "description": ""
        },
        {
            "id": "MONDO:0030608",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030608",
            "name": "interstitial lung disease 1",
            "description": ""
        },
        {
            "id": "MIM:619611",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619611",
            "name": "Interstitial lung disease 1",
            "description": "Interstitial lung disease 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060941"
    ],
    "unlinked_id_list": []
}