{
    "disease_id": "DOID:0110836", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013935", 
            "name": "CIB2 Usher syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013935", 
            "name": "USH1J"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013935", 
            "name": "Usher syndrome type Ij"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013935", 
            "name": "USHER syndrome, type Ij; USH1J"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013935", 
            "name": "USHER syndrome, type Ij"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013935", 
            "name": "Usher syndrome, type 1J"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013935", 
            "name": "Usher syndrome caused by mutation in CIB2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110836", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110836", 
            "name": "USH1J"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110836", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110836", 
            "name": "Usher syndrome type IJ"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110836", 
        "description": "An Usher syndrome type 1 that has_material_basis_in caused by homozygous mutation in the CIB2 gene on chromosome 15q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110836", 
        "name": "Usher syndrome type 1J"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110836#disease-associations", 
            "id": "0110836", 
            "database": "Alliance of Genome Resources"
        }
    ]
}