{
    "disease_id": "DOID:0090036",
    "recommended_name": {
        "id": "DOID:0090036",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0090036",
        "name": "myoclonic dystonia 26",
        "description": "A myoclonic dystonia characterized by onset of myoclonic jerks affecting the upper limbs, progressing to dystonia with predominant involvement of the craniocervical regions, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the KCTD17 gene on chromosome 22q12."
    },
    "synonyms": [
        {
            "id": "MONDO:0014620",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014620",
            "name": "myoclonic dystonia 26",
            "description": "Any myoclonus-dystonia syndrome in which the cause of the disease is a mutation in the KCTD17 gene."
        },
        {
            "id": "MONDO:0014620",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014620",
            "name": "myoclonus-dystonia syndrome caused by mutation in KCTD17",
            "description": ""
        },
        {
            "id": "MONDO:0014620",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014620",
            "name": "dystonia 26, myoclonic",
            "description": ""
        },
        {
            "id": "MONDO:0014620",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014620",
            "name": "dystonia 26, myoclonic; DYT26",
            "description": ""
        },
        {
            "id": "MONDO:0014620",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014620",
            "name": "DYT26",
            "description": ""
        },
        {
            "id": "MONDO:0014620",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014620",
            "name": "myoclonic dystonia type 26",
            "description": ""
        },
        {
            "id": "MONDO:0014620",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014620",
            "name": "KCTD17 myoclonus-dystonia syndrome",
            "description": ""
        },
        {
            "id": "MIM:616398",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616398",
            "name": "Dystonia 26, myoclonic",
            "description": "Dystonia 26, myoclonic"
        }
    ]
}