{
    "disease_id": "DOID:0110541", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007424", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007424", 
            "name": "deafness, progressive Low tone"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007424", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007424", 
            "name": "deafness, autosomal dominant 1; DFNA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007424", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007424", 
            "name": "deafness, autosomal dominant 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007424", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007424", 
            "name": "autosomal dominant deafness 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007424", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007424", 
            "name": "DIAPH1 autosomal dominant nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007424", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007424", 
            "name": "deafness, autosomal dominant type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007424", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007424", 
            "name": "hereditary low frequency hearing loss 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007424", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007424", 
            "name": "autosomal dominant nonsyndromic deafness type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007424", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007424", 
            "name": "DFNA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007424", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007424", 
            "name": "deafness, autosomal dominant 1, with or without thrombocytopenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007424", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007424", 
            "name": "LFHL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007424", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007424", 
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in DIAPH1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007424", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007424", 
            "name": "hereditary Low frequency hearing loss"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007424", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007424", 
            "name": "Konigsmark syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110541", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110541", 
            "name": "DFNA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110541", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110541", 
            "name": "Konigsmark syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110541", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110541", 
            "name": "LFHL1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110541", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110541", 
            "name": "autosomal dominant deafness 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110541", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110541", 
            "name": "hereditary low frequency hearing loss 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110541", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110541", 
            "name": "autosomal dominant deafness 1, with or without thrombocytopenia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110541", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110541", 
        "name": "autosomal dominant nonsyndromic deafness 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110541#disease-associations", 
            "id": "0110541", 
            "database": "Alliance of Genome Resources"
        }
    ]
}