{
    "disease_id": "DOID:0110215",
    "recommended_name": {
        "id": "DOID:0110215",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110215",
        "name": "Leber congenital amaurosis 5",
        "description": "A Leber congenital amaurosis that is characterized by severe visual dysfunction, nystagmus, the oculodigital sign, and a normal fundus with onset in infancy and has_material_basis_in mutation in the LCA5 gene on chromosome 6q14.1."
    },
    "synonyms": [
        {
            "id": "DOID:0110215",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110215",
            "name": "LCA5",
            "description": ""
        },
        {
            "id": "MONDO:0011473",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011473",
            "name": "Leber congenital amaurosis 5",
            "description": "Any Leber congenital amaurosis in which the cause of the disease is a mutation in the LCA5 gene."
        },
        {
            "id": "MONDO:0011473",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011473",
            "name": "LCA5",
            "description": ""
        },
        {
            "id": "MONDO:0011473",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011473",
            "name": "LCA5 Leber congenital amaurosis",
            "description": ""
        },
        {
            "id": "MONDO:0011473",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011473",
            "name": "Leber congenital amaurosis 5",
            "description": ""
        },
        {
            "id": "MONDO:0011473",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011473",
            "name": "Leber congenital amaurosis caused by mutation in LCA5",
            "description": ""
        },
        {
            "id": "MONDO:0011473",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011473",
            "name": "Leber congenital amaurosis type 5",
            "description": ""
        },
        {
            "id": "MONDO:0011473",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011473",
            "name": "amaurosis congenita of Leber, type 5",
            "description": ""
        },
        {
            "id": "MIM:604537",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604537",
            "name": "Leber congenital amaurosis 5",
            "description": "Leber congenital amaurosis 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110215"
    ],
    "unlinked_id_list": []
}