{
    "disease_id": "DOID:0090048", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012789", 
            "name": "dystonia type 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012789", 
            "name": "PRKRA dystonic disorder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012789", 
            "name": "dystonia 16; DYT16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012789", 
            "name": "dystonic disorder caused by mutation in PRKRA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012789", 
            "name": "Young-onset dystonia-(parkinsonism)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012789", 
            "name": "DYT-PRKRA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012789", 
            "name": "early-onset dystonia parkinsonism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012789", 
            "name": "DYT16"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090048", 
        "description": "A multifocal dystonia that is characterized by early-onset progressive limb dystonia, laryngeal and oromandibular dystonia, and parkinsonism, and that has_material_basis_in autosomal recessive inheritance of homozygous mutation in the protein activator of interferon induced protein kinase EIF2AK2 (PRKRA) gene on chromosome 2q31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090048", 
        "name": "dystonia 16"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/612067", 
            "id": "612067", 
            "database": "MIM"
        }
    ]
}