{
    "disease_id": "DOID:0110629",
    "recommended_name": {
        "id": "DOID:0110629",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110629",
        "name": "Wolfram syndrome 1",
        "description": "An autosomal recessive disease that is characterized by diabetes mellitus, optic atrophy, and deafness as well as various other possible disorders and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the WFS1 gene on chromosome 4p16.1."
    },
    "synonyms": [
        {
            "id": "DOID:0110629",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110629",
            "name": "DIDMOAD",
            "description": ""
        },
        {
            "id": "DOID:0110629",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110629",
            "name": "WFS1",
            "description": ""
        },
        {
            "id": "DOID:0110629",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110629",
            "name": "diabetes mellitus AND insipidus with optic atrophy AND deafness",
            "description": ""
        },
        {
            "id": "MONDO:0009101",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009101",
            "name": "Wolfram syndrome 1",
            "description": "Any Wolfram syndrome in which the cause of the disease is a mutation in the WFS1 gene."
        },
        {
            "id": "MONDO:0009101",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009101",
            "name": "Wolfram syndrome caused by mutation in WFS1",
            "description": ""
        },
        {
            "id": "MONDO:0009101",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009101",
            "name": "diabetes insipidus and mellitus with optic atrophy and deafness",
            "description": ""
        },
        {
            "id": "MONDO:0009101",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009101",
            "name": "WOLFRAM syndrome 1; WFS1",
            "description": ""
        },
        {
            "id": "MONDO:0009101",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009101",
            "name": "Wolfram syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0009101",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009101",
            "name": "Wfs",
            "description": ""
        },
        {
            "id": "MONDO:0009101",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009101",
            "name": "Wolfram syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009101",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009101",
            "name": "WFS1",
            "description": ""
        },
        {
            "id": "MONDO:0009101",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009101",
            "name": "WFS1 Wolfram syndrome",
            "description": ""
        },
        {
            "id": "MIM:222300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/222300",
            "name": "Wolfram syndrome 1",
            "description": "Wolfram syndrome 1"
        }
    ]
}