{
    "disease_id": "DOID:397", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007270", 
            "name": "cardiomyopathy, familial restrictive, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007270", 
            "name": "cardiomyopathy, familial restrictive, 1; RCM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007270", 
            "name": "RCM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007270", 
            "name": "familial isolated restrictive cardiomyopathy caused by mutation in TNNI3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007270", 
            "name": "cardiomyopathy, familial restrictive, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007270", 
            "name": "Rcm"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007270", 
            "name": "TNNI3 familial isolated restrictive cardiomyopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:397", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:397", 
            "name": "Cardiomyopathy, constrictive"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:397", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:397", 
            "name": "primary restrictive cardiomyopathy"
        }, 
        {
            "url": "https://www.omim.org/entry/115210", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:115210", 
            "name": "Cardiomyopathy, familial restrictive 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:397", 
        "description": "An intrinsic cardiomyopathy characterized by impaired ventricular filling, with normal or decreased diastolic volume of either or both ventricles typically resulting from increased stiffness of the myocardium.", 
        "resource": "Disease Ontology", 
        "id": "DOID:397", 
        "name": "restrictive cardiomyopathy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/115210", 
            "id": "115210", 
            "database": "MIM"
        }
    ]
}