{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012003", 
            "name": "deafness, autosomal recessive 39"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012003", 
            "name": "HGF autosomal recessive nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012003", 
            "name": "DFNB39"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012003", 
            "name": "autosomal recessive deafness 39"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012003", 
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in HGF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012003", 
            "name": "deafness, autosomal recessive 39; DFNB39"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012003", 
            "name": "deafness, autosomal recessive type 39"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012003", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012003", 
            "name": "autosomal recessive nonsyndromic deafness type 39"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110497", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110497", 
            "name": "DFNB39"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110497", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110497", 
            "name": "autosomal recessive deafness 39"
        }, 
        {
            "url": "https://www.omim.org/entry/608265", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:608265", 
            "name": "Deafness, autosomal recessive, 39"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110497", 
        "description": "An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110497", 
        "name": "autosomal recessive nonsyndromic deafness 39"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/608265", 
            "id": "608265", 
            "database": "MIM"
        }
    ]
}