{
    "disease_id": "DOID:0110515", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012670", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012670", 
            "name": "deafness, autosomal recessive 63"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012670", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012670", 
            "name": "deafness, autosomal recessive 63; DFNB63"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012670", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012670", 
            "name": "LRTOMT autosomal recessive nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012670", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012670", 
            "name": "autosomal recessive deafness 63"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012670", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012670", 
            "name": "DFNB63"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012670", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012670", 
            "name": "deafness, autosomal recessive type 63"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012670", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012670", 
            "name": "autosomal recessive nonsyndromic deafness type 63"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012670", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012670", 
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in LRTOMT"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110515", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110515", 
            "name": "DFNB63"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110515", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110515", 
            "name": "autosomal recessive deafness 63"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110515", 
        "description": "An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the LRTOMT gene on chromosome 11q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110515", 
        "name": "autosomal recessive nonsyndromic deafness 63"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110515#disease-associations", 
            "id": "0110515", 
            "database": "Alliance of Genome Resources"
        }
    ]
}