{
    "disease_id": "DOID:0080583",
    "recommended_name": {
        "id": "DOID:0080583",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080583",
        "name": "Wolfram syndrome, mitochondrial form",
        "description": "A Wolfram syndrome that has_material_basis_in mutation in mtDNA."
    },
    "synonyms": [
        {
            "id": "DOID:0080583",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080583",
            "name": "DIDMOAD, mitochondrial form",
            "description": ""
        },
        {
            "id": "DOID:0080583",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080583",
            "name": "diabetes mellitus AND insipidus with optic atrophy AND deafness mitochondrial form",
            "description": ""
        },
        {
            "id": "MONDO:0010800",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010800",
            "name": "Wolfram syndrome, mitochondrial form",
            "description": ""
        },
        {
            "id": "MONDO:0010800",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010800",
            "name": "Didmoad syndrome, mitochondrial form",
            "description": ""
        },
        {
            "id": "MONDO:0010800",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010800",
            "name": "diabetes insipidus and mellitus with optic atrophy and deafness, mitochondrial form",
            "description": ""
        },
        {
            "id": "MONDO:0010800",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010800",
            "name": "Wolfram syndrome, mitochondrial form",
            "description": ""
        }
    ]
}