{
    "disease_id": "DOID:0070676",
    "recommended_name": {
        "id": "DOID:0070676",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070676",
        "name": "autosomal recessive nonsyndromic deafness 124",
        "description": "An autosomal recessive nonsyndromic deafness characterized by congenital progressive sensorineural hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in the PKHD1L1 gene on chromosome 8q23."
    },
    "synonyms": [
        {
            "id": "DOID:0070676",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070676",
            "name": "DFNB124",
            "description": ""
        },
        {
            "id": "DOID:0070676",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070676",
            "name": "autosomal recessive deafness 124",
            "description": ""
        },
        {
            "id": "MONDO:0968981",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0968981",
            "name": "autosomal recessive nonsyndromic hearing loss 124",
            "description": ""
        },
        {
            "id": "MONDO:0968981",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0968981",
            "name": "deafness, autosomal recessive 124",
            "description": ""
        },
        {
            "id": "MIM:620794",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620794",
            "name": "Deafness, autosomal recessive, 124",
            "description": "Deafness, autosomal recessive, 124"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070676"
    ],
    "unlinked_id_list": []
}