{
    "disease_id": "DOID:0050995",
    "recommended_name": {
        "id": "DOID:0050995",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050995",
        "name": "episodic ataxia type 7",
        "description": "An episodic ataxia that is characterized by episodes of weakness and dysarthria, and has_material_basis_in autosomal dominant inheritance."
    },
    "synonyms": [
        {
            "id": "MONDO:0012755",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012755",
            "name": "episodic ataxia type 7",
            "description": "Episodic ataxia type 7 (EA7) is an exceedingly rare form of Hereditary episodic ataxia (see this term) characterized by ataxia with weakness, vertigo, and dysarthria without interictal findings."
        },
        {
            "id": "MONDO:0012755",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012755",
            "name": "episodic ataxia, type 7; EA7",
            "description": ""
        },
        {
            "id": "MONDO:0012755",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012755",
            "name": "episodic ataxia, type 7",
            "description": ""
        },
        {
            "id": "MONDO:0012755",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012755",
            "name": "EA7",
            "description": ""
        }
    ]
}