{
    "disease_id": "DOID:0060650", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009110", 
            "name": "dicarboxylic aminoaciduria; DCBXA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009110", 
            "name": "Dicarboxylicaminoaciduria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009110", 
            "name": "DCBXA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009110", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009110", 
            "name": "glutamate-aspartate Transport defect"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060650", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060650", 
            "name": "glutamate-aspartate transport defect"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060650", 
        "description": "An amino acid metabolic disorder that is characterised by an excess urinary excretion of aspartate and glutamate acidic amino acids.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060650", 
        "name": "dicarboxylic aminoaciduria"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060650#disease-associations", 
            "id": "0060650", 
            "database": "Alliance of Genome Resources"
        }
    ]
}