{
    "disease_id": "DOID:0080109", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014122", 
            "name": "myofibromatosis, infantile, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014122", 
            "name": "myofibromatosis caused by mutation in NOTCH3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014122", 
            "name": "myofibromatosis, infantile, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014122", 
            "name": "IMF2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014122", 
            "name": "NOTCH3 myofibromatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014122", 
            "name": "myofibromatosis, infantile, 2; IMF2"
        }, 
        {
            "url": "https://www.omim.org/entry/615293", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615293", 
            "name": "Myofibromatosis, infantile 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080109", 
        "description": "A connective tissue benign neoplasm that is characterized by the development of benign tumors in the skin, striated muscles, bones, and in exceptional cases, visceral organs.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080109", 
        "name": "infantile myofibromatosis"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615293", 
            "id": "615293", 
            "database": "MIM"
        }
    ]
}