{
    "disease_id": "DOID:0050996", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014476", 
            "name": "episodic ataxia type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014476", 
            "name": "EA8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014476", 
            "name": "episodic ataxia with slurred speech"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014476", 
            "name": "episodic ataxia, type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014476", 
            "name": "episodic ataxia type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014476", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014476", 
            "name": "episodic ataxia, type 8; EA8"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050996", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050996", 
        "name": "episodic ataxia type 8"
    }
}