{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010983", 
            "name": "choreoathetosis/spasticity, episodic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010983", 
            "name": "dystonia type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010983", 
            "name": "Cse choreoathetosis, paroxysmal, with episodic ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010983", 
            "name": "dystonia 9; DYT9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010983", 
            "name": "choreoathetosis, kinesigenic, with episodic ataxia and spasticity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010983", 
            "name": "DYT9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010983", 
            "name": "episodic choreoathetosis/spasticity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010983", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010983", 
            "name": "paroxysmal dystonic choreathetosis with episodic ataxia and spasticity"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090044", 
        "description": "A dystonia that is characterized by paroxysmal choreoathetosis and progressive spastic paraplegia, with episodes often precipitated by alcohol, fatigue, or emotional stress, and that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 2 member 1 (SLC2A1) gene on chromosome 1p34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090044", 
        "name": "dystonia 9"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/601042", 
            "id": "601042", 
            "database": "MIM"
        }
    ]
}