{
    "disease_id": "DOID:0050573",
    "recommended_name": {
        "id": "DOID:0050573",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050573",
        "name": "2-hydroxyglutaric aciduria",
        "description": "An amino acid metabolic disorder that is an autosomal recessive neurometabolic disorder characterized by the significant elevation of urinary levels of hydroxyglutaric acid causing progressive brain damage."
    },
    "synonyms": [],
    "children": [
        {
            "id": "DOID:0050574",
            "label": "L-2-hydroxyglutaric aciduria",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050575",
            "label": "D-2-hydroxyglutaric aciduria",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0111351",
                    "label": "D-2-hydroxyglutaric aciduria 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111352",
                    "label": "D-2-hydroxyglutaric aciduria 2",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0111619",
            "label": "combined D-2- and L-2-hydroxyglutaric aciduria",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0050575",
        "DOID:0111619",
        "DOID:0111351",
        "DOID:0111352",
        "DOID:0050574",
        "DOID:0050573"
    ],
    "unlinked_id_list": []
}