{
    "disease_id": "DOID:0060693", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010379", 
            "name": "Brunner syndrome; BRNRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010379", 
            "name": "monoamine oxidase A deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010379", 
            "name": "antisocial behavior, susceptibility to"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010379", 
            "name": "BRNRS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060693", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060693", 
            "name": "monoamine oxidase A deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060693", 
        "description": "An amino acid metabolic disorder characterized by recessive X-linked inhetiance, impaired monoamine metabolism, impulsive aggressiveness and mild mental retardation that has_material_basis_in mutation in the MAOA gene on chromosome Xp11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060693", 
        "name": "Brunner Syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060693#disease-associations", 
            "id": "0060693", 
            "database": "Alliance of Genome Resources"
        }
    ]
}