{
    "disease_id": "DOID:0110033", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008762", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008762", 
            "name": "Alport syndrome, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008762", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008762", 
            "name": "Alport syndrome autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008762", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008762", 
            "name": "Alport syndrome recessive type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008762", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008762", 
            "name": "nephropathy and deafness"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110033", 
        "description": "An Alport syndrome that has_material -basis_in homozygous or compound heterozygous mutation in the COL4A3 or the COL4A4 gene, both of which map to chromosome 2q.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110033", 
        "name": "autosomal recessive Alport syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110033#disease-associations", 
            "id": "0110033", 
            "database": "Alliance of Genome Resources"
        }
    ]
}