{
    "disease_id": "DOID:0110497",
    "recommended_name": {
        "id": "DOID:0110497",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110497",
        "name": "autosomal recessive nonsyndromic deafness 39",
        "description": "An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110497",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110497",
            "name": "DFNB39",
            "description": ""
        },
        {
            "id": "DOID:0110497",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110497",
            "name": "autosomal recessive deafness 39",
            "description": ""
        },
        {
            "id": "MONDO:0012003",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012003",
            "name": "autosomal recessive nonsyndromic deafness 39",
            "description": "An autosomal recessive disorder caused by mutations in the HGF gene, encoding hepatocyte growth factor receptor. It is characterized by profound deafness."
        },
        {
            "id": "MONDO:0012003",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012003",
            "name": "deafness, autosomal recessive 39",
            "description": ""
        },
        {
            "id": "MONDO:0012003",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012003",
            "name": "HGF autosomal recessive nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0012003",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012003",
            "name": "DFNB39",
            "description": ""
        },
        {
            "id": "MONDO:0012003",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012003",
            "name": "autosomal recessive deafness 39",
            "description": ""
        },
        {
            "id": "MONDO:0012003",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012003",
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in HGF",
            "description": ""
        },
        {
            "id": "MONDO:0012003",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012003",
            "name": "deafness, autosomal recessive 39; DFNB39",
            "description": ""
        },
        {
            "id": "MONDO:0012003",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012003",
            "name": "deafness, autosomal recessive type 39",
            "description": ""
        },
        {
            "id": "MONDO:0012003",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012003",
            "name": "autosomal recessive nonsyndromic deafness type 39",
            "description": ""
        },
        {
            "id": "MIM:608265",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608265",
            "name": "Deafness, autosomal recessive, 39",
            "description": "Deafness, autosomal recessive, 39"
        }
    ]
}