{
    "disease_id": "DOID:0050694",
    "recommended_name": {
        "id": "DOID:0050694",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050694",
        "name": "Brown-Vialetto-Van Laere syndrome",
        "description": "A syndrome that is characterized by sensorineural hearing loss and a variety of cranial nerve palsies, usually involving the motor components of the seventh and ninth to twelfth cranial nerves."
    },
    "synonyms": [
        {
            "id": "MONDO:0024537",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024537",
            "name": "Brown-Vialetto-van Laere syndrome 1",
            "description": "Any Brown-Vialetto-van Laere syndrome in which the cause of the disease is a mutation in the SLC52A3 gene."
        },
        {
            "id": "MONDO:0024537",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024537",
            "name": "Brown-Vialetto-Van Laere syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0024537",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024537",
            "name": "Brown-Vialetto-van Laere syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0024537",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024537",
            "name": "Brown-Vialetto-van Laere syndrome caused by mutation in SLC52A3",
            "description": ""
        },
        {
            "id": "MONDO:0024537",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024537",
            "name": "RTD2",
            "description": ""
        },
        {
            "id": "MONDO:0024537",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024537",
            "name": "Riboflavin transporter deficiency 2",
            "description": ""
        },
        {
            "id": "MONDO:0024537",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024537",
            "name": "SLC52A3 Brown-Vialetto-van Laere syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0024537",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024537",
            "name": "rfvt2-related riboflavin transporter deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0024537",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024537",
            "name": "BVVLS1",
            "description": ""
        },
        {
            "id": "MIM:211530",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/211530",
            "name": "Brown-Vialetto-Van Laere syndrome 1",
            "description": "Brown-Vialetto-Van Laere syndrome 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0080785",
            "label": "Brown-Vialetto-Van Laere syndrome 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0080786",
            "label": "Brown-Vialetto-Van Laere syndrome 2",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0080786",
        "DOID:0050694",
        "DOID:0080785"
    ],
    "unlinked_id_list": []
}