{
    "disease_id": "DOID:0110016",
    "recommended_name": {
        "id": "DOID:0110016",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110016",
        "name": "Leber congenital amaurosis 2",
        "description": "A Leber congenital amaurosis that is characterized by night blindness, some transient improvement in vision, and eventual progressive visual loss and has_material_basis_in mutation in the RPE65 gene on chromosome 1."
    },
    "synonyms": [
        {
            "id": "DOID:0110016",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110016",
            "name": "LCA2",
            "description": ""
        },
        {
            "id": "DOID:0110016",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110016",
            "name": "amaurosis congenita of Leber II",
            "description": ""
        },
        {
            "id": "MONDO:0008765",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008765",
            "name": "Leber congenital amaurosis 2",
            "description": "Any Leber congenital amaurosis in which the cause of the disease is a mutation in the RPE65 gene."
        },
        {
            "id": "MONDO:0008765",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008765",
            "name": "LCA2",
            "description": ""
        },
        {
            "id": "MONDO:0008765",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008765",
            "name": "Leber congenital amaurosis 2",
            "description": ""
        },
        {
            "id": "MONDO:0008765",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008765",
            "name": "Leber congenital amaurosis caused by mutation in RPE65",
            "description": ""
        },
        {
            "id": "MONDO:0008765",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008765",
            "name": "Leber congenital amaurosis type 2",
            "description": ""
        },
        {
            "id": "MONDO:0008765",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008765",
            "name": "RPE65 Leber congenital amaurosis",
            "description": ""
        },
        {
            "id": "MONDO:0008765",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008765",
            "name": "amaurosis congenita of Leber, type 2",
            "description": ""
        },
        {
            "id": "MIM:204100",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/204100",
            "name": "Leber congenital amaurosis 2",
            "description": "Leber congenital amaurosis 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110016"
    ],
    "unlinked_id_list": []
}