{
    "disease_id": "DOID:0090055", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014033", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014033", 
            "name": "dystonia type 25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014033", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014033", 
            "name": "dystonia 25; DYT25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014033", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014033", 
            "name": "dystonic disorder caused by mutation in GNAL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014033", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014033", 
            "name": "autosomal dominant focal dystonia, DYT25 type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014033", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014033", 
            "name": "DYT25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014033", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014033", 
            "name": "GNAL dystonic disorder"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090055", 
        "description": "A multifocal dystonia that is characterized by cervical, laryngeal and hand-forearm dystonia, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the GNAL gene on chromosome 18p11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090055", 
        "name": "dystonia 25"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615073", 
            "id": "615073", 
            "database": "MIM"
        }
    ]
}