{
    "disease_id": "DOID:0112168",
    "recommended_name": {
        "id": "DOID:0112168",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112168",
        "name": "autosomal dominant nonsyndromic deafness 77",
        "description": "An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the ABCC1 gene on chromosome 16p13.11."
    },
    "synonyms": [
        {
            "id": "DOID:0112168",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112168",
            "name": "DFNA77",
            "description": ""
        },
        {
            "id": "MONDO:0030058",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030058",
            "name": "hearing loss, autosomal dominant 77",
            "description": ""
        },
        {
            "id": "MONDO:0030058",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030058",
            "name": "DFNA77",
            "description": ""
        },
        {
            "id": "MONDO:0030058",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030058",
            "name": "deafness, autosomal dominant 77",
            "description": ""
        },
        {
            "id": "MIM:618915",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618915",
            "name": "Deafness, autosomal dominant, 77",
            "description": "Deafness, autosomal dominant, 77"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112168"
    ],
    "unlinked_id_list": []
}