{
    "disease_id": "DOID:0080096", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012289", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012289", 
            "name": "myofibrillar myopathy (disease) caused by mutation in FLNC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012289", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012289", 
            "name": "myopathy, myofibrillar, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012289", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012289", 
            "name": "filaminopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012289", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012289", 
            "name": "muscle filaminopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012289", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012289", 
            "name": "myopathy, myofibrillar, 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012289", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012289", 
            "name": "FLNC myofibrillar myopathy (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012289", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012289", 
            "name": "myopathy, myofibrillar, 5; MFM5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012289", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012289", 
            "name": "myopathy, myofibrillar, filamin C-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012289", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012289", 
            "name": "MFM5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012289", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012289", 
            "name": "myofibrillar myopathy type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012289", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012289", 
            "name": "filaminopathy, autosomal dominant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080096", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080096", 
            "name": "filaminopathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080096", 
        "description": "A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the FLNC gene on chromosome 7q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080096", 
        "name": "myofibrillar myopathy 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080096#disease-associations", 
            "id": "0080096", 
            "database": "Alliance of Genome Resources"
        }
    ]
}