{
    "disease_id": "DOID:0110521", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013978", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013978", 
            "name": "deafness, autosomal recessive type 70"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013978", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013978", 
            "name": "autosomal recessive nonsyndromic deafness type 70"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013978", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013978", 
            "name": "deafness, autosomal recessive 70"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013978", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013978", 
            "name": "PNPT1 autosomal recessive nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013978", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013978", 
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in PNPT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013978", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013978", 
            "name": "deafness, autosomal recessive 70; DFNB70"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013978", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013978", 
            "name": "DFNB70"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013978", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013978", 
            "name": "autosomal recessive deafness 70"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110521", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110521", 
            "name": "DFNB70"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110521", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110521", 
            "name": "autosomal recessive deafness 70"
        }, 
        {
            "url": "https://www.omim.org/entry/614934", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614934", 
            "name": "Deafness, autosomal recessive, 70"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110521", 
        "description": "An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the PNPT1 gene on chromosome 2p16.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110521", 
        "name": "autosomal recessive nonsyndromic deafness 70"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614934", 
            "id": "614934", 
            "database": "MIM"
        }
    ]
}