{
    "disease_id": "DOID:0110541",
    "recommended_name": {
        "id": "DOID:0110541",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110541",
        "name": "autosomal dominant nonsyndromic deafness 1",
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by low frequency progressive hearing loss and has_material_basis_in mutation in the DIAPH1 gene on chromosome 5q31."
    },
    "synonyms": [
        {
            "id": "DOID:0110541",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110541",
            "name": "DFNA1",
            "description": ""
        },
        {
            "id": "DOID:0110541",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110541",
            "name": "Konigsmark syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110541",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110541",
            "name": "LFHL1",
            "description": ""
        },
        {
            "id": "DOID:0110541",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110541",
            "name": "autosomal dominant deafness 1",
            "description": ""
        },
        {
            "id": "DOID:0110541",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110541",
            "name": "hereditary low frequency hearing loss 1",
            "description": ""
        },
        {
            "id": "DOID:0110541",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110541",
            "name": "autosomal dominant deafness 1, with or without thrombocytopenia",
            "description": ""
        },
        {
            "id": "MONDO:0007424",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007424",
            "name": "autosomal dominant nonsyndromic hearing loss 1",
            "description": "Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the DIAPH1 gene."
        },
        {
            "id": "MONDO:0007424",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007424",
            "name": "Konigsmark syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007424",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007424",
            "name": "DFNA1",
            "description": ""
        },
        {
            "id": "MONDO:0007424",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007424",
            "name": "DIAPH1 autosomal dominant nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0007424",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007424",
            "name": "autosomal dominant deafness 1",
            "description": ""
        },
        {
            "id": "MONDO:0007424",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007424",
            "name": "autosomal dominant nonsyndromic deafness 1",
            "description": ""
        },
        {
            "id": "MONDO:0007424",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007424",
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in DIAPH1",
            "description": ""
        },
        {
            "id": "MONDO:0007424",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007424",
            "name": "autosomal dominant nonsyndromic deafness type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007424",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007424",
            "name": "deafness, autosomal dominant 1",
            "description": ""
        },
        {
            "id": "MONDO:0007424",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007424",
            "name": "deafness, autosomal dominant 1, with or without thrombocytopenia",
            "description": ""
        },
        {
            "id": "MONDO:0007424",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007424",
            "name": "deafness, autosomal dominant type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007424",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007424",
            "name": "deafness, progressive Low tone",
            "description": ""
        },
        {
            "id": "MIM:124900",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/124900",
            "name": "Deafness, autosomal dominant 1, with or without thrombocytopenia",
            "description": "Deafness, autosomal dominant 1, with or without thrombocytopenia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110541"
    ],
    "unlinked_id_list": []
}