{
    "disease_id": "DOID:0111453", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008774", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008774", 
            "name": "AMOXAD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008774", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008774", 
            "name": "Alpha-aminoadipic aciduria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008774", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008774", 
            "name": "2-aminoadipic 2-oxoadipic aciduria; AMOXAD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111453", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111453", 
            "name": "AMOXAD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111453", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111453", 
            "name": "alpha-aminoadipic aciduria"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111453", 
        "description": "An amino acid metabolic disorder characterized by defects in L-lysine degradation resulting in variable neurological symptoms but in many cases patients are asymptomatic that has _material_basis_in homozygous or compound heterozygous mutation in DHTKD1 on chromosome 10p14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111453", 
        "name": "2-aminoadipic 2-oxoadipic aciduria"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111453#disease-associations", 
            "id": "0111453", 
            "database": "Alliance of Genome Resources"
        }
    ]
}