{
    "disease_id": "DOID:2754", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "GSD type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "GSD6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "glycogenosis type VI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "liver glycogen phosphorylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "PYGL glycogen storage disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "GSD due to liver glycogen phosphorylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "glycogen storage disease type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "phosphorylase deficiency glycogen-storage disease of liver"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "glycogenosis type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "glycogen storage disease due to liver glycogen phosphorylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "GSD type VI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "hers disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "hepatic glycogen phosphorylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "glycogen storage disease caused by mutation in PYGL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "hepatic phosphorylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "hers' disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "glycogenosis due to liver glycogen phosphorylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "glycogen storage disease VI; GSD6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "GSD 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "glycogen storage disease 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "hepatophosphorylase deficiency glycogenosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009294", 
            "name": "glycogen storage disease type VI"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2754", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2754", 
            "name": "Hers' disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2754", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2754", 
            "name": "glycogen storage disease type VI"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2754", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2754", 
            "name": "hepatic glycogen phosphorylase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2754", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2754", 
            "name": "hepatophosphorylase deficiency glycogenosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2754", 
        "description": "A glycogen storage disease characterized by enlargement of the liver, moderately low blood sugar, elevated levels of acetone and other ketone bodies in the blood and moderate growth retardation.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2754", 
        "name": "glycogen storage disease VI"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/2754#disease-associations", 
            "id": "2754", 
            "database": "Alliance of Genome Resources"
        }
    ]
}