{
    "disease_id": "DOID:0110513",
    "recommended_name": {
        "id": "DOID:0110513",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110513",
        "name": "autosomal recessive nonsyndromic deafness 61",
        "description": "An autosomal recessive nonsyndromic deafness that is characterized by early childhood-onset moderate to severe sensorineural hearing loss and has_material_basis_in mutation in the SLC26A5 gene on chromosome 7q22."
    },
    "synonyms": [
        {
            "id": "DOID:0110513",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110513",
            "name": "DFNB61",
            "description": ""
        },
        {
            "id": "DOID:0110513",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110513",
            "name": "autosomal recessive deafness 61",
            "description": ""
        },
        {
            "id": "MONDO:0013471",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013471",
            "name": "autosomal recessive nonsyndromic hearing loss 61",
            "description": "Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the SLC26A5 gene."
        },
        {
            "id": "MONDO:0013471",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013471",
            "name": "DFNB61",
            "description": ""
        },
        {
            "id": "MONDO:0013471",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013471",
            "name": "SLC26A5 autosomal recessive nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0013471",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013471",
            "name": "autosomal recessive deafness 61",
            "description": ""
        },
        {
            "id": "MONDO:0013471",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013471",
            "name": "autosomal recessive nonsyndromic deafness 61",
            "description": ""
        },
        {
            "id": "MONDO:0013471",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013471",
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in SLC26A5",
            "description": ""
        },
        {
            "id": "MONDO:0013471",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013471",
            "name": "autosomal recessive nonsyndromic deafness type 61",
            "description": ""
        },
        {
            "id": "MONDO:0013471",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013471",
            "name": "deafness, autosomal recessive 61",
            "description": ""
        },
        {
            "id": "MONDO:0013471",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013471",
            "name": "deafness, autosomal recessive type 61",
            "description": ""
        },
        {
            "id": "MIM:613865",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613865",
            "name": "Deafness, autosomal recessive, 61",
            "description": "Deafness, autosomal recessive, 61"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110513"
    ],
    "unlinked_id_list": []
}