{
    "disease_id": "DOID:0110511",
    "recommended_name": {
        "id": "DOID:0110511",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110511",
        "name": "autosomal recessive nonsyndromic deafness 59",
        "description": "An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the DFNB59 gene on chromosome 2q31."
    },
    "synonyms": [
        {
            "id": "DOID:0110511",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110511",
            "name": "DFNB59",
            "description": ""
        },
        {
            "id": "DOID:0110511",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110511",
            "name": "autosomal recessive deafness 59",
            "description": ""
        },
        {
            "id": "MONDO:0012445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012445",
            "name": "autosomal recessive nonsyndromic hearing loss 59",
            "description": "Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the PJVK gene."
        },
        {
            "id": "MONDO:0012445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012445",
            "name": "autosomal recessive nonsyndromic hearing loss 59",
            "description": ""
        },
        {
            "id": "MONDO:0012445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012445",
            "name": "DFNB59",
            "description": ""
        },
        {
            "id": "MONDO:0012445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012445",
            "name": "PJVK autosomal recessive nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0012445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012445",
            "name": "autosomal recessive deafness 59",
            "description": ""
        },
        {
            "id": "MONDO:0012445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012445",
            "name": "autosomal recessive nonsyndromic deafness 59",
            "description": ""
        },
        {
            "id": "MONDO:0012445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012445",
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in PJVK",
            "description": ""
        },
        {
            "id": "MONDO:0012445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012445",
            "name": "autosomal recessive nonsyndromic deafness type 59",
            "description": ""
        },
        {
            "id": "MONDO:0012445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012445",
            "name": "deafness, autosomal recessive 59",
            "description": ""
        },
        {
            "id": "MONDO:0012445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012445",
            "name": "deafness, autosomal recessive type 59",
            "description": ""
        },
        {
            "id": "MIM:610220",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/610220",
            "name": "Deafness, autosomal recessive, 59",
            "description": "Deafness, autosomal recessive, 59"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110511"
    ],
    "unlinked_id_list": []
}