{
    "disease_id": "DOID:0050437",
    "recommended_name": {
        "id": "DOID:0050437",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050437",
        "name": "Danon disease",
        "description": "A lysosomal storage disease that is characterized by cardiomyopathy, skeletal myopathy and intellectual disability and has_material_basis_in mutations in the LAMP2 gene."
    },
    "synonyms": [
        {
            "id": "DOID:0050437",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050437",
            "name": "ANTOPOL DISEASE",
            "description": ""
        },
        {
            "id": "DOID:0050437",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050437",
            "name": "PSEUDOGLYCOGENOSIS II",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "Danon disease",
            "description": "A lysosomal glycogen storage disease characterized by severe cardiomyopathy and variable degrees of muscle weakness, frequently associated with intellectual deficit."
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "ANTOPOL disease",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "Danon disease",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "Danon disease, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "GSD due to LAMP-2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "LAMP2 lysosomal glycogen storage disease",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "glycogen storage disease type IIb",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "glycogenosis due to LAMP-2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "lysosomal glycogen storage disease caused by mutation in LAMP2",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "lysosomal glycogen storage disease with normal acid maltase activity",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "GSD IIb",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "GSD2B (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "X-linked vacuolar cardiomyopathy and myopathy",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "glycogen storage cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "glycogen storage disease limited to the heart",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "glycogen storage disease type 2b (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "lysosomal glycogen storage disease without acid maltase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "lysosomal glycogen storage disease without acid maltase deficiency (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0010281",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010281",
            "name": "vacuolar cardiomyopathy and myopathy X-linked",
            "description": ""
        },
        {
            "id": "MIM:300257",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300257",
            "name": "Danon disease",
            "description": "Danon disease"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050437"
    ],
    "unlinked_id_list": []
}