{
    "disease_id": "DOID:0090056", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007496", 
            "name": "dystonia-Parkinsonism, rapid-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007496", 
            "name": "RDP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007496", 
            "name": "ATP1A3 dystonic disorder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007496", 
            "name": "rapid-onset dystonia-parkinsonism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007496", 
            "name": "DYT12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007496", 
            "name": "dystonia 12; DYT12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007496", 
            "name": "dystonia type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007496", 
            "name": "dystonic disorder caused by mutation in ATP1A3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007496", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007496", 
            "name": "DYT-ATP1A3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090056", 
        "description": "A dystonia that is characterized by asymmetric dystonia and parkinsonism with abrupt onset in young adulthood that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the gene encoding the alpha-3 subunit of the N,K-ATPase (ATP1A3) on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090056", 
        "name": "dystonia 12"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090056#disease-associations", 
            "id": "0090056", 
            "database": "Alliance of Genome Resources"
        }
    ]
}