{
    "disease_id": "DOID:0080098", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014922", 
            "name": "myofibrillar myopathy (disease) caused by mutation in KY"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014922", 
            "name": "myopathy, myofibrillar, type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014922", 
            "name": "MFM7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014922", 
            "name": "KY myofibrillar myopathy (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014922", 
            "name": "alpha-b crystalin-related fatal infantile hypertonic myofibrillar myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014922", 
            "name": "myopathy, myofibrillar, 7; MFM7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014922", 
            "name": "myopathy, myofibrillar, 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080098", 
        "description": "A myofibrillar myopathy that has_material_basis_in homozygous mutation in the KY gene on chromosome 3q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080098", 
        "name": "myofibrillar myopathy 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080098#disease-associations", 
            "id": "0080098", 
            "database": "Alliance of Genome Resources"
        }
    ]
}