{
    "disease_id": "DOID:0110567", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011994", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011994", 
            "name": "autosomal dominant nonsyndromic deafness type 41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011994", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011994", 
            "name": "autosomal dominant deafness 41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011994", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011994", 
            "name": "deafness, autosomal dominant 41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011994", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011994", 
            "name": "P2RX2 autosomal dominant nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011994", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011994", 
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in P2RX2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011994", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011994", 
            "name": "deafness, autosomal dominant 41; DFNA41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011994", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011994", 
            "name": "deafness, autosomal dominant type 41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011994", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011994", 
            "name": "DFNA41"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110567", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110567", 
            "name": "DFNA41"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110567", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110567", 
            "name": "autosomal dominant deafness 41"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110567", 
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat progressive hearing loss and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the purinergic receptor P2X 2 gene (P2RX2) on chromosome 12q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110567", 
        "name": "autosomal dominant nonsyndromic deafness 41"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110567#disease-associations", 
            "id": "0110567", 
            "database": "Alliance of Genome Resources"
        }
    ]
}