{
    "disease_id": "DOID:0081295",
    "recommended_name": {
        "id": "DOID:0081295",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081295",
        "name": "essential tremor 6",
        "description": "An essential tremor that is characterized by adult-onset kinetic and/or postural tremor usually affecting the upper limbs and that has_material_basis_in heterozygous trinucleotide GGC repeat expansion in the 5-prime untranslated region of the NOTCH2NLC gene on chromosome 1q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0030027",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030027",
            "name": "tremor, hereditary essential, 6",
            "description": ""
        },
        {
            "id": "MONDO:0030027",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030027",
            "name": "ETM6",
            "description": ""
        },
        {
            "id": "MONDO:0030027",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030027",
            "name": "TREMOR, HEREDITARY ESSENTIAL, 6",
            "description": ""
        },
        {
            "id": "MONDO:0030027",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030027",
            "name": "tremor, hereditary essential, 6",
            "description": ""
        },
        {
            "id": "MIM:618866",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618866",
            "name": "Tremor, hereditary essential 6",
            "description": "Tremor, hereditary essential 6"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081295"
    ],
    "unlinked_id_list": []
}