{
    "disease_id": "DOID:0110476",
    "recommended_name": {
        "id": "DOID:0110476",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110476",
        "name": "autosomal recessive nonsyndromic deafness 1B",
        "description": "An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has_material_basis_in mutation in the GJB6 gene on chromosome 13q12."
    },
    "synonyms": [
        {
            "id": "DOID:0110476",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110476",
            "name": "DFNB1B",
            "description": ""
        },
        {
            "id": "DOID:0110476",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110476",
            "name": "autosomal recessive deafness 1B",
            "description": ""
        },
        {
            "id": "MONDO:0012977",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012977",
            "name": "autosomal recessive nonsyndromic hearing loss 1B",
            "description": "Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the GJB6 gene."
        },
        {
            "id": "MONDO:0012977",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012977",
            "name": "Autosomal recessive deafness type 1B",
            "description": ""
        },
        {
            "id": "MONDO:0012977",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012977",
            "name": "DFNB1B",
            "description": ""
        },
        {
            "id": "MONDO:0012977",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012977",
            "name": "GJB6 autosomal recessive nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0012977",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012977",
            "name": "autosomal recessive deafness 1B",
            "description": ""
        },
        {
            "id": "MONDO:0012977",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012977",
            "name": "autosomal recessive nonsyndromic deafness 1B",
            "description": ""
        },
        {
            "id": "MONDO:0012977",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012977",
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in GJB6",
            "description": ""
        },
        {
            "id": "MONDO:0012977",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012977",
            "name": "autosomal recessive nonsyndromic deafness type 1B",
            "description": ""
        },
        {
            "id": "MONDO:0012977",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012977",
            "name": "deafness, autosomal recessive 1B",
            "description": ""
        },
        {
            "id": "MONDO:0012977",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012977",
            "name": "deafness, autosomal recessive 1b",
            "description": ""
        },
        {
            "id": "MONDO:0012977",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012977",
            "name": "deafness, autosomal recessive type 1B",
            "description": ""
        },
        {
            "id": "MIM:612645",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612645",
            "name": "Deafness, autosomal recessive, 1B",
            "description": "Deafness, autosomal recessive, 1B"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110476"
    ],
    "unlinked_id_list": []
}