{
    "disease_id": "DOID:0110732",
    "recommended_name": {
        "id": "DOID:0110732",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110732",
        "name": "neuronal ceroid lipofuscinosis 11",
        "description": "A neuronal ceroid lipofuscinosis that is characterized by autosomal recessive inheritance with rapidly progressive visual loss due to retinal dystrophy, seizures, cerebellar ataxia, and cerebellar atrophy and has_material_basis_in homozygous mutation in the GRN gene on chromosome 17q."
    },
    "synonyms": [
        {
            "id": "DOID:0110732",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110732",
            "name": "CLN11",
            "description": ""
        },
        {
            "id": "MONDO:0013866",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013866",
            "name": "neuronal ceroid lipofuscinosis 11",
            "description": "Any neuronal ceroid lipofuscinosis in which the cause of the disease is a mutation in the GRN gene."
        },
        {
            "id": "MONDO:0013866",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013866",
            "name": "CLN11",
            "description": ""
        },
        {
            "id": "MONDO:0013866",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013866",
            "name": "GRN neuronal ceroid lipofuscinosis",
            "description": ""
        },
        {
            "id": "MONDO:0013866",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013866",
            "name": "Grn neuronal ceroid lipofuscinosis",
            "description": ""
        },
        {
            "id": "MONDO:0013866",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013866",
            "name": "ceroid lipofuscinosis, neuronal, type 11",
            "description": ""
        },
        {
            "id": "MONDO:0013866",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013866",
            "name": "neuronal ceroid lipofuscinosis caused by mutation in GRN",
            "description": ""
        },
        {
            "id": "MONDO:0013866",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013866",
            "name": "neuronal ceroid lipofuscinosis caused by mutation in Grn",
            "description": ""
        },
        {
            "id": "MONDO:0013866",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013866",
            "name": "neuronal ceroid lipofuscinosis type 11",
            "description": ""
        },
        {
            "id": "MONDO:0013866",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013866",
            "name": "ceroid lipofuscinosis, neuronal, 11",
            "description": ""
        },
        {
            "id": "MIM:614706",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614706",
            "name": "Ceroid lipofuscinosis, neuronal, 11",
            "description": "Ceroid lipofuscinosis, neuronal, 11"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110732"
    ],
    "unlinked_id_list": []
}