{
    "disease_id": "DOID:0110629", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009101", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009101", 
            "name": "Wolfram syndrome caused by mutation in WFS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009101", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009101", 
            "name": "diabetes insipidus and mellitus with optic atrophy and deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009101", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009101", 
            "name": "WOLFRAM syndrome 1; WFS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009101", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009101", 
            "name": "Wfs"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009101", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009101", 
            "name": "Wolfram syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009101", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009101", 
            "name": "WFS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009101", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009101", 
            "name": "WFS1 Wolfram syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110629", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110629", 
            "name": "DIDMOAD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110629", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110629", 
            "name": "WFS1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110629", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110629", 
            "name": "diabetes mellitus AND insipidus with optic atrophy AND deafness"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110629", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110629", 
        "name": "Wolfram syndrome 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110629#disease-associations", 
            "id": "0110629", 
            "database": "Alliance of Genome Resources"
        }
    ]
}