{
    "disease_id": "DOID:0090053", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007494", 
            "name": "paroxysmal kinesigenic choreathetosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007494", 
            "name": "episodic kinesigenic dyskinesia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007494", 
            "name": "PRRT2 episodic kinesigenic dyskinesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007494", 
            "name": "paroxysmal kinesigenic dyskinesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007494", 
            "name": "dystonia, familial paroxysmal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007494", 
            "name": "paroxysmal kinesigenic choreoathetosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007494", 
            "name": "DYT-PRRT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007494", 
            "name": "dystonia 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007494", 
            "name": "episodic kinesigenic dyskinesia caused by mutation in PRRT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007494", 
            "name": "familial PKD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007494", 
            "name": "episodic kinesigenic dyskinesia 1; EKD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007494", 
            "name": "PxMD-PRRT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007494", 
            "name": "familial paroxysmal kinesigenic dyskinesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007494", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007494", 
            "name": "EKD1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090053", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090053", 
            "name": "Paroxysmal kinesigenic choreoathetosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090053", 
        "description": "A dystonia characterized by recurrent brief involuntary hyperkinesias triggered by sudden movements that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the proline-rich transmembrane protein 2 gene (PRRT2) on chromosome 16p11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090053", 
        "name": "episodic kinesigenic dyskinesia 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090053#disease-associations", 
            "id": "0090053", 
            "database": "Alliance of Genome Resources"
        }
    ]
}