{
    "disease_id": "DOID:0110834", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011748", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011748", 
            "name": "Usher syndrome type Ig"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011748", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011748", 
            "name": "USHER syndrome, type Ig"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011748", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011748", 
            "name": "Usher syndrome, type 1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011748", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011748", 
            "name": "USH1G Usher syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011748", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011748", 
            "name": "Usher syndrome caused by mutation in USH1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011748", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011748", 
            "name": "USH1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011748", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011748", 
            "name": "USHER syndrome, type Ig; USH1G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110834", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110834", 
            "name": "USH1G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110834", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110834", 
            "name": "Usher syndrome type IG"
        }, 
        {
            "url": "https://www.omim.org/entry/606943", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:606943", 
            "name": "Usher syndrome 1G"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110834", 
        "description": "An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110834", 
        "name": "Usher syndrome type 1G"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/606943", 
            "id": "606943", 
            "database": "MIM"
        }
    ]
}