{
    "disease_id": "DOID:0080584",
    "recommended_name": {
        "id": "DOID:0080584",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080584",
        "name": "autosomal dominant Wolfram syndrome",
        "description": "A Wolfram syndrome that is characterized by congenital progressive hearing impairment, diabetes mellitus, and optic atrophy and that has_material_basis_in autosomal dominant inheritance of a heterozygous mutation in the WFS1 gene on chromosome 4p16."
    },
    "synonyms": [
        {
            "id": "MONDO:0013673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013673",
            "name": "Wolfram-like syndrome",
            "description": "Wolfram-like syndrome is a rare endocrine disease characterized by the triad of adult-onset diabetes mellitus, progressive hearing loss (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy. Psychiatric (i.e. anxiety, depression, hallucinations) and sleep disorders, the only neurologic abnormalities observed in this disease, have been reported in rare cases. Unlike Wolfram syndrome, patients with Wolfram-like syndrome do not report endocrine or cardiac findings."
        },
        {
            "id": "MONDO:0013673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013673",
            "name": "Wolfram-like syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013673",
            "name": "WFSL",
            "description": ""
        },
        {
            "id": "MONDO:0013673",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013673",
            "name": "Wolfram-like syndrome, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:614296",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614296",
            "name": "Wolfram-like syndrome autosomal dominant",
            "description": "Wolfram-like syndrome autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080584"
    ],
    "unlinked_id_list": []
}