{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010984", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010984", 
            "name": "USH1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010984", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010984", 
            "name": "Usher syndrome, type 1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010984", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010984", 
            "name": "Ush1D/F, Cdh23/Pcdh15, digenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010984", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010984", 
            "name": "USHER syndrome, type ID; USH1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010984", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010984", 
            "name": "Usher syndrome, type Id/F, Cdh23/Pcdh15, digenic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010984", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010984", 
            "name": "Usher syndrome type ID"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010984", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010984", 
            "name": "USHER syndrome, type ID"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110831", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110831", 
            "name": "USH1D"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110831", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110831", 
            "name": "Usher syndrome type ID"
        }, 
        {
            "url": "https://www.omim.org/entry/601067", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:601067", 
            "name": "Usher syndrome 1D"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110831", 
        "description": "An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110831", 
        "name": "Usher syndrome type 1D"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/601067", 
            "id": "601067", 
            "database": "MIM"
        }
    ]
}