{
    "disease_id": "DOID:0090035",
    "recommended_name": {
        "id": "DOID:0090035",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0090035",
        "name": "myoclonic dystonia 15",
        "description": "A myoclonic dystonia that is characterized by jerky movements of the upper limbs, hands, and axial muscles, and has_material_basis_in autosomal dominant inheritance of variation in the chromosome region 18p11."
    },
    "synonyms": [
        {
            "id": "MONDO:0011844",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011844",
            "name": "myoclonic dystonia 15",
            "description": "A myoclonic dystonia characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 18p11."
        },
        {
            "id": "MONDO:0011844",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011844",
            "name": "dystonia-15, myoclonic",
            "description": ""
        },
        {
            "id": "MONDO:0011844",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011844",
            "name": "myoclonic dystonia type 15",
            "description": ""
        },
        {
            "id": "MONDO:0011844",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011844",
            "name": "DYT15",
            "description": ""
        },
        {
            "id": "MONDO:0011844",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011844",
            "name": "dystonia 15, myoclonic",
            "description": ""
        }
    ]
}