{
    "disease_id": "DOID:0110838", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010169", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010169", 
            "name": "US2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010169", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010169", 
            "name": "Usher syndrome, type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010169", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010169", 
            "name": "USHER syndrome, type IIA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010169", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010169", 
            "name": "USH2A Usher syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010169", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010169", 
            "name": "Usher syndrome caused by mutation in USH2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010169", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010169", 
            "name": "Usher syndrome type IIA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010169", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010169", 
            "name": "USH2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010169", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010169", 
            "name": "USHER syndrome, type IIA; USH2A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110838", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110838", 
            "name": "USH2A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110838", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110838", 
            "name": "Usher syndrome type IIA"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110838", 
        "description": "An Usher syndrome type 2 characterized by moderate to severe sensorineural hearing loss, mainly affecting perception of high frequency sounds and progressive retinitis pigmentosa that has_material_basis_in homozygous or compound heterozygous mutation in the USH2A gene on chromosome 1q41.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110838", 
        "name": "Usher syndrome type 2A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110838#disease-associations", 
            "id": "0110838", 
            "database": "Alliance of Genome Resources"
        }
    ]
}