{
    "disease_id": "DOID:0090036", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014620", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014620", 
            "name": "myoclonus-dystonia syndrome caused by mutation in KCTD17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014620", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014620", 
            "name": "dystonia 26, myoclonic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014620", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014620", 
            "name": "dystonia 26, myoclonic; DYT26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014620", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014620", 
            "name": "DYT26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014620", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014620", 
            "name": "myoclonic dystonia type 26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014620", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014620", 
            "name": "KCTD17 myoclonus-dystonia syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090036", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090036", 
        "name": "myoclonic dystonia 26"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090036#disease-associations", 
            "id": "0090036", 
            "database": "Alliance of Genome Resources"
        }
    ]
}