{
    "disease_id": "DOID:0090101", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009867", 
            "name": "fatal congenital hypertrophic cardiomyopathy due to glycogenosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009867", 
            "name": "fatal congenital nonlysosomal cardiac glycogenosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009867", 
            "name": "glycogen storage disease of heart"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009867", 
            "name": "glycogen storage disease caused by mutation in PRKAG2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009867", 
            "name": "phosphorylase kinase deficiency of heart"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009867", 
            "name": "glycogen storage disease of heart, lethal congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009867", 
            "name": "fatal congenital hypertrophic cardiomyopathy due to GSD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009867", 
            "name": "PRKAG2 glycogen storage disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009867", 
            "name": "fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090101", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090101", 
            "name": "fatal congenital hypertrophic cardiomyopathy due to GSD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090101", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090101", 
            "name": "fatal congenital nonlysosomal cardiac glycogenosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090101", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090101", 
            "name": "phosphorylase kinase deficiency of heart"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090101", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090101", 
            "name": "fatal congenital hypertrophic cardiomyopathy due to glycogenosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090101", 
        "description": "A glycogen storage disease characterized by glycogenosis confined to the heart, hypoglycemia and cyanosis, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the gene encoding the noncatalytic gamma-2 subunit of AMP-activated protein kinase (PRKAG2) on chromosome 7q36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090101", 
        "name": "lethal congenital glycogen storage disease of heart"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090101#disease-associations", 
            "id": "0090101", 
            "database": "Alliance of Genome Resources"
        }
    ]
}