{
    "disease_id": "DOID:0110436", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011702", 
            "name": "dilated cardiomyopathy type 1L"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011702", 
            "name": "CMD1L"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011702", 
            "name": "SGCD familial isolated dilated cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011702", 
            "name": "familial isolated dilated cardiomyopathy caused by mutation in SGCD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011702", 
            "name": "cardiomyopathy, dilated, type 1L"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011702", 
            "name": "cardiomyopathy, dilated, 1L"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011702", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011702", 
            "name": "cardiomyopathy, dilated, 1L; CMD1L"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110436", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110436", 
            "name": "CMD1L"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110436", 
        "description": "A dilated cardiomyopathy that has_material_basis_in mutations in the SGCD gene on chromosome 5q33.2-q33.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110436", 
        "name": "dilated cardiomyopathy 1L"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110436#disease-associations", 
            "id": "0110436", 
            "database": "Alliance of Genome Resources"
        }
    ]
}