{
    "disease_id": "DOID:0111427",
    "recommended_name": {
        "id": "DOID:0111427",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111427",
        "name": "restrictive cardiomyopathy 3",
        "description": "A restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in TNNT2 on chromosome 1q32.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111427",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111427",
            "name": "RCM3",
            "description": ""
        },
        {
            "id": "DOID:0111427",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111427",
            "name": "familial restrictive cardiomyopathy 3",
            "description": ""
        },
        {
            "id": "MONDO:0012900",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012900",
            "name": "cardiomyopathy, familial restrictive, 3",
            "description": "Any familial isolated restrictive cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene."
        },
        {
            "id": "MONDO:0012900",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012900",
            "name": "cardiomyopathy, familial restrictive, 3; RCM3",
            "description": ""
        },
        {
            "id": "MONDO:0012900",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012900",
            "name": "familial isolated restrictive cardiomyopathy caused by mutation in TNNT2",
            "description": ""
        },
        {
            "id": "MONDO:0012900",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012900",
            "name": "TNNT2 familial isolated restrictive cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0012900",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012900",
            "name": "RCM3",
            "description": ""
        },
        {
            "id": "MONDO:0012900",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012900",
            "name": "cardiomyopathy, familial restrictive, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0012900",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012900",
            "name": "cardiomyopathy, familial restrictive, 3",
            "description": ""
        },
        {
            "id": "MIM:612422",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612422",
            "name": "Cardiomyopathy, familial restrictive 3",
            "description": "Cardiomyopathy, familial restrictive 3"
        }
    ]
}