{
    "disease_id": "DOID:0050760", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010684", 
            "name": "XMEA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010684", 
            "name": "MEAX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010684", 
            "name": "vacuolar myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010684", 
            "name": "myopathy, X-linked, with excessive autophagy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010684", 
            "name": "myopathy, X-linked, with excessive autophagy; MEAX"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050760", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050760", 
            "name": "XMEA"
        }, 
        {
            "url": "https://www.omim.org/entry/310440", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:310440", 
            "name": "Myopathy, X-linked, with excessive autophagy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050760", 
        "description": "A myopathy that is characterized by childhood onset of progressive muscle weakness and atrophy primarily affecting the proximal muscles in males between 5 and 10 years old, has_material_basis_in mutation in the VMA21 gene on chromosome Xq28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050760", 
        "name": "X-linked myopathy with excessive autophagy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/310440", 
            "id": "310440", 
            "database": "MIM"
        }
    ]
}