{
    "disease_id": "DOID:0111427", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012900", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012900", 
            "name": "cardiomyopathy, familial restrictive, 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012900", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012900", 
            "name": "cardiomyopathy, familial restrictive, 3; RCM3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012900", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012900", 
            "name": "familial isolated restrictive cardiomyopathy caused by mutation in TNNT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012900", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012900", 
            "name": "TNNT2 familial isolated restrictive cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012900", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012900", 
            "name": "RCM3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012900", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012900", 
            "name": "cardiomyopathy, familial restrictive, type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111427", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111427", 
            "name": "RCM3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111427", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111427", 
            "name": "familial restrictive cardiomyopathy 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111427", 
        "description": "A restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in TNNT2 on chromosome 1q32.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111427", 
        "name": "restrictive cardiomyopathy 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111427#disease-associations", 
            "id": "0111427", 
            "database": "Alliance of Genome Resources"
        }
    ]
}