{
    "disease_id": "DOID:0110826", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010168", 
            "name": "Usher syndrome, type I, French variety"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010168", 
            "name": "USH1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010168", 
            "name": "retinitis pigmentosa and congenital deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010168", 
            "name": "Usher syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010168", 
            "name": "Usher syndrome, type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010168", 
            "name": "Usher syndrome, type Ia, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010168", 
            "name": "Usher syndrome, type Ia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010168", 
            "name": "USHER syndrome, type I; USH1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010168", 
            "name": "USHER syndrome, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010168", 
            "name": "Usher syndrome, type I, French variety, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010168", 
            "name": "US1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010168", 
            "name": "Usher syndrome, type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010168", 
            "name": "USH1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110826", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110826", 
            "name": "US1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110826", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110826", 
            "name": "USH1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110826", 
        "description": "An Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110826", 
        "name": "Usher syndrome type 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110826#disease-associations", 
            "id": "0110826", 
            "database": "Alliance of Genome Resources"
        }
    ]
}