{
    "disease_id": "DOID:0110331",
    "recommended_name": {
        "id": "DOID:0110331",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110331",
        "name": "Leber congenital amaurosis 3",
        "description": "A Leber congenital amaurosis that has_material_basis_in mutation in the SPATA7 gene on chromosome 14q31."
    },
    "synonyms": [
        {
            "id": "DOID:0110331",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110331",
            "name": "LCA3",
            "description": ""
        },
        {
            "id": "MONDO:0011415",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011415",
            "name": "Leber congenital amaurosis 3",
            "description": "Any Leber congenital amaurosis in which the cause of the disease is a mutation in the SPATA7 gene."
        },
        {
            "id": "MONDO:0011415",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011415",
            "name": "Leber congenital amaurosis caused by mutation in SPATA7",
            "description": ""
        },
        {
            "id": "MONDO:0011415",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011415",
            "name": "Leber congenital amaurosis 3",
            "description": ""
        },
        {
            "id": "MONDO:0011415",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011415",
            "name": "retinitis pigmentosa, juvenile, Spata7-related",
            "description": ""
        },
        {
            "id": "MONDO:0011415",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011415",
            "name": "Leber congenital amaurosis 3; LCA3",
            "description": ""
        },
        {
            "id": "MONDO:0011415",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011415",
            "name": "amaurosis congenita of Leber, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011415",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011415",
            "name": "LCA3",
            "description": ""
        },
        {
            "id": "MONDO:0011415",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011415",
            "name": "Leber congenital amaurosis type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011415",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011415",
            "name": "SPATA7 Leber congenital amaurosis",
            "description": ""
        },
        {
            "id": "MIM:604232",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604232",
            "name": "Leber congenital amaurosis 3",
            "description": "Leber congenital amaurosis 3"
        }
    ]
}