{
    "disease_id": "DOID:0111444", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009699", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009699", 
            "name": "action myoclonus-renal failure syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009699", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009699", 
            "name": "myoclonus-nephropathy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009699", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009699", 
            "name": "AMRF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009699", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009699", 
            "name": "progressive myoclonic epilepsy type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009699", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009699", 
            "name": "epilepsy, progressive myoclonic, 4, with or without renal failure"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009699", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009699", 
            "name": "epilepsy, progressive myoclonic, 4, with or without renal failure; EPM4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009699", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009699", 
            "name": "EPM4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111444", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111444", 
            "name": "AMRF"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111444", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111444", 
            "name": "EPM4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111444", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111444", 
            "name": "Myoclonus-nephropathy syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111444", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111444", 
            "name": "action myoclonus-renal failure syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111444", 
        "description": "A progressive myoclonus epilepsy characterized by progressive myoclonic epilepsy often associated with renal failure that has_material_basis_in homozygous or compound heterozygous of mutation in SCARB2 on chromosome 4q21.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111444", 
        "name": "progressive myoclonus epilepsy 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111444#disease-associations", 
            "id": "0111444", 
            "database": "Alliance of Genome Resources"
        }
    ]
}