{
    "disease_id": "DOID:2749", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009287", 
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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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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009287", 
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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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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009287", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009287", 
            "name": "glycogen storage disease caused by mutation in G6PC"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009287", 
            "name": "G6PC glycogen storage disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009287", 
            "name": "G6P deficiency type 1a"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009287", 
            "name": "glucose-6-phosphatase deficiency glycogen storage disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009287", 
            "name": "GSD type 1a"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009287", 
            "name": "glycogen storage disease Ia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009287", 
            "name": "glycogen storage disease type 1a"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009287", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "glycogenosis type Ia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009287", 
            "name": "glycogen storage disease 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2749", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2749", 
            "name": "Glycogen storage disease, type I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2749", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2749", 
            "name": "deficiency of glucose-6-phosphatase"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2749", 
            "name": "glycogen storage disease type I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2749", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2749", 
            "name": "glycogenosis type I"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2749", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2749", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2749", 
            "name": "von Gierke's disease"
        }, 
        {
            "url": "https://www.omim.org/entry/232200", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:232200", 
            "name": "Glycogen storage disease 1A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2749", 
        "description": "A glycogen storage disease that has_material_basis_in deficiency of the glucose-6-phosphatase enzyme which impairs the ability of the liver to produce free glucose from glycogen and from gluconeogenesis and is characterized by accumulation of glycogen and fat in the liver and kidneys, resulting in hepatomegaly and renomegaly.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2749", 
        "name": "glycogen storage disease I"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/232200", 
            "id": "232200", 
            "database": "MIM"
        }
    ]
}