{
    "disease_id": "DOID:0110188",
    "recommended_name": {
        "id": "DOID:0110188",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110188",
        "name": "Leber congenital amaurosis 14",
        "description": "A Leber congenital amaurosis that has_material_basis_in mutation in the LRAT gene on chromosome 4q31."
    },
    "synonyms": [
        {
            "id": "DOID:0110188",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110188",
            "name": "LCA14",
            "description": ""
        },
        {
            "id": "MONDO:0013231",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013231",
            "name": "Leber congenital amaurosis 14",
            "description": "Any Leber congenital amaurosis in which the cause of the disease is a mutation in the LRAT gene."
        },
        {
            "id": "MONDO:0013231",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013231",
            "name": "LCA14",
            "description": ""
        },
        {
            "id": "MONDO:0013231",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013231",
            "name": "LRAT Leber congenital amaurosis",
            "description": ""
        },
        {
            "id": "MONDO:0013231",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013231",
            "name": "Leber congenital amaurosis 14",
            "description": ""
        },
        {
            "id": "MONDO:0013231",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013231",
            "name": "Leber congenital amaurosis caused by mutation in LRAT",
            "description": ""
        },
        {
            "id": "MONDO:0013231",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013231",
            "name": "Leber congenital amaurosis type 14",
            "description": ""
        },
        {
            "id": "MONDO:0013231",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013231",
            "name": "retinal dystrophy, early-onset severe",
            "description": ""
        },
        {
            "id": "MIM:613341",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613341",
            "name": "Leber congenital amaurosis 14",
            "description": "Leber congenital amaurosis 14"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110188"
    ],
    "unlinked_id_list": []
}