{
    "disease_id": "DOID:0110566",
    "recommended_name": {
        "id": "DOID:0110566",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110566",
        "name": "autosomal dominant nonsyndromic deafness 40",
        "description": "An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CRYM gene on chromosome 16p12."
    },
    "synonyms": [
        {
            "id": "DOID:0110566",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110566",
            "name": "DFNA40",
            "description": ""
        },
        {
            "id": "DOID:0110566",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110566",
            "name": "autosomal dominant deafness 40",
            "description": ""
        },
        {
            "id": "MONDO:0014603",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014603",
            "name": "autosomal dominant nonsyndromic hearing loss 40",
            "description": "Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the CRYM gene."
        },
        {
            "id": "MONDO:0014603",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014603",
            "name": "autosomal dominant nonsyndromic hearing loss 40",
            "description": ""
        },
        {
            "id": "MONDO:0014603",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014603",
            "name": "CRYM autosomal dominant nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0014603",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014603",
            "name": "DFNA40",
            "description": ""
        },
        {
            "id": "MONDO:0014603",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014603",
            "name": "autosomal dominant deafness 40",
            "description": ""
        },
        {
            "id": "MONDO:0014603",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014603",
            "name": "autosomal dominant nonsyndromic deafness 40",
            "description": ""
        },
        {
            "id": "MONDO:0014603",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014603",
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in CRYM",
            "description": ""
        },
        {
            "id": "MONDO:0014603",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014603",
            "name": "autosomal dominant nonsyndromic deafness type 40",
            "description": ""
        },
        {
            "id": "MONDO:0014603",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014603",
            "name": "deafness, autosomal dominant 40",
            "description": ""
        },
        {
            "id": "MONDO:0014603",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014603",
            "name": "deafness, autosomal dominant type 40",
            "description": ""
        },
        {
            "id": "MIM:616357",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616357",
            "name": "Deafness, autosomal dominant, 40",
            "description": "Deafness, autosomal dominant, 40"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110566"
    ],
    "unlinked_id_list": []
}