{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009708", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009708", 
            "name": "myopathy, myosin storage, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009708", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009708", 
            "name": "myopathy, myosin storage, autosomal recessive; MSMB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009708", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009708", 
            "name": "MSMB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009708", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009708", 
            "name": "myopathy, hyaline body, autosomal recessive"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111268", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111268", 
            "name": "MSMB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111268", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111268", 
            "name": "Myopathy, myosin storage, autosomal recessive"
        }, 
        {
            "url": "https://www.omim.org/entry/255160", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:255160", 
            "name": "Myopathy, myosin storage, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111268", 
        "description": "A hyaline body myopathy that has_material_basis_in compound heterozygous or homozygous mutation in MYH7 on 14q11.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111268", 
        "name": "autosomal recessive hyaline body myopathy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/255160", 
            "id": "255160", 
            "database": "MIM"
        }
    ]
}