{
    "disease_id": "DOID:0081298",
    "recommended_name": {
        "id": "DOID:0081298",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0081298",
        "name": "oculopharyngodistal myopathy 2",
        "description": "An oculopharyngodistal myopathy that is characterized by onset of distal muscle weakness, mainly of the lower limbs, and/or ophthalmoplegia in the second or third decades of life, and that has_material_basis_in heterozygous trinucleotide repeat expansion (GGC(n)) in the 5-prime untranslated region (UTR) of the GIPC1 gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0030134",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030134",
            "name": "oculopharyngodistal myopathy 2",
            "description": ""
        },
        {
            "id": "MONDO:0030134",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030134",
            "name": "OCULOPHARYNGODISTAL MYOPATHY 2",
            "description": ""
        },
        {
            "id": "MONDO:0030134",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030134",
            "name": "OPDM2",
            "description": ""
        },
        {
            "id": "MONDO:0030134",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030134",
            "name": "oculopharyngodistal myopathy 2",
            "description": ""
        },
        {
            "id": "MIM:618940",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618940",
            "name": "Oculopharyngodistal myopathy 2",
            "description": "Oculopharyngodistal myopathy 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081298"
    ],
    "unlinked_id_list": []
}