{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011400", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011400", 
            "name": "cardiomyopathy, dilated, 1G; CMD1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011400", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011400", 
            "name": "cardiomyopathy, dilated, 1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011400", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011400", 
            "name": "CMD1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011400", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011400", 
            "name": "familial isolated dilated cardiomyopathy caused by mutation in TTN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011400", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011400", 
            "name": "dilated cardiomyopathy type 1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011400", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011400", 
            "name": "TTN familial isolated dilated cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011400", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011400", 
            "name": "cardiomyopathy, dilated, type 1G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110430", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110430", 
            "name": "CMD1G"
        }, 
        {
            "url": "https://www.omim.org/entry/604145", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:604145", 
            "name": "Cardiomyopathy, dilated 1G"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110430", 
        "description": "A dilated cardiomyopathy that has_material_basis_in mutation in the TTN gene on chromosome 2q31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110430", 
        "name": "dilated cardiomyopathy 1G"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/604145", 
            "id": "604145", 
            "database": "MIM"
        }
    ]
}