{
    "disease_id": "DOID:0050996",
    "recommended_name": {
        "id": "DOID:0050996",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050996",
        "name": "episodic ataxia type 8",
        "description": "An episodic ataxia that is characterized by weakness, dysarthria and myokymia, and has_material_basis_in autosomal dominant inheritance of mutation in the UBR4 gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0014476",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014476",
            "name": "episodic ataxia type 8",
            "description": ""
        },
        {
            "id": "MONDO:0014476",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014476",
            "name": "episodic ataxia with slurred speech",
            "description": ""
        },
        {
            "id": "MONDO:0014476",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014476",
            "name": "EA8",
            "description": ""
        },
        {
            "id": "MONDO:0014476",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014476",
            "name": "episodic ataxia, type 8; EA8",
            "description": ""
        },
        {
            "id": "MONDO:0014476",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014476",
            "name": "episodic ataxia type 8",
            "description": ""
        },
        {
            "id": "MONDO:0014476",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014476",
            "name": "episodic ataxia, type 8",
            "description": ""
        }
    ]
}