{
    "disease_id": "DOID:2746", 
    "synonyms": [
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            "description": "", 
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        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009293", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
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            "description": "", 
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        }, 
        {
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            "description": "", 
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        }, 
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "glycogen storage disease due to muscle glycogen phosphorylase deficiency"
        }, 
        {
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            "description": "", 
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        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009293", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009293", 
            "name": "Pygm deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009293", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009293", 
            "name": "McArdle type glycogen storage disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2746", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2746", 
            "name": "Glycogen storage disease, type V"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2746", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2746", 
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            "description": "", 
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            "id": "DOID:2746", 
            "name": "glycogen storage disease type V"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2746", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2746", 
            "name": "myophosphorylase deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2746", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:2746", 
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    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/2746#disease-associations", 
            "id": "2746", 
            "database": "Alliance of Genome Resources"
        }
    ]
}