{
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    "synonyms": [
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            "description": "", 
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        {
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            "description": "", 
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "cirrhosis, familial, with deposition of abnormal glycogen"
        }, 
        {
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            "description": "", 
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        {
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            "description": "", 
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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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        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009292", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009292", 
            "name": "amylopectinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009292", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009292", 
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        {
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            "description": "", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009292", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "GSD IV, neuromuscular form, fatal perinatal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009292", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009292", 
            "name": "branching-transferase deficiency glycogenosis"
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        {
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            "description": "", 
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
            "resource": "MONDO", 
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            "name": "GSD type IV"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009292", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "glycogen storage disease 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009292", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "GSD IV, neuromuscular form, congenital"
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        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "GSD due to glycogen branching enzyme deficiency"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "brancher deficiency"
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        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "GSD IV, classic hepatic"
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        {
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "resource": "MONDO", 
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            "name": "glycogen branching enzyme deficiency"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009292", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "deficiency of 1,4-alpha-glucan branching enzyme"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009292", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009292", 
            "name": "glycogen storage disease caused by mutation in GBE1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009292", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009292", 
            "name": "GSD IV, nonprogressive hepatic"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2750", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2750", 
            "name": "Amylopectinosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2750", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2750", 
            "name": "Branching-transferase deficiency glycogenosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2750", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2750", 
            "name": "Glycogen storage disease, type IV"
        }, 
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            "url": "http://disease-ontology.org/term/DOID:2750", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2750", 
            "name": "brancher deficiency glycogenosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2750", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2750", 
            "name": "deficiency of 1,4-alpha-glucan branching enzyme"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2750", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:2750", 
        "name": "glycogen storage disease IV"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/2750#disease-associations", 
            "id": "2750", 
            "database": "Alliance of Genome Resources"
        }
    ]
}