{
    "disease_id": "DOID:0090049", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "paroxysmal nonkinesigenic dyskinesia 1; PNKD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "Paroxysomal nonkinesigenic dyskinesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "paroxysmal non-kinesigenic dyskinesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "paroxysmal dyskinesia caused by mutation in PNKD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "choreoathetosis, nonkinesigenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "PNKD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "dystonia 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "mount-reback syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "PNKD paroxysmal dyskinesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "Paroxystic non-kinesigenic choreoathetosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "choreoathetosis, familial paroxysmal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "DYT-MR-1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "PxMD-PNKD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "paroxysmal nonkinesigenic dyskinesia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007326", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007326", 
            "name": "paroxysmal dystonic choreoathetosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090049", 
        "description": "A dystonia that is characterized by attacks of dystonic or choreathetotic movements precipitated by stress, fatigue, coffee or alcohol intake or menstruation, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the PNKD metallo-beta-lactamase domain containing gene on chromosome 2q35.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090049", 
        "name": "paroxysmal nonkinesigenic dyskinesia 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090049#disease-associations", 
            "id": "0090049", 
            "database": "Alliance of Genome Resources"
        }
    ]
}