{
    "disease_id": "DOID:0110727",
    "recommended_name": {
        "id": "DOID:0110727",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110727",
        "name": "neuronal ceroid lipofuscinosis 13",
        "description": "A neuronal ceroid lipofuscinosis that is characterized by autosomal recessive inheritance with adult onset of progressive cognitive decline and motor dysfunction leading to dementia and often early death and has_material_basis_in homozygous or compound heterozygous mutation in the CTSF gene on chromosome 11q13."
    },
    "synonyms": [
        {
            "id": "DOID:0110727",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110727",
            "name": "CLN13",
            "description": ""
        },
        {
            "id": "DOID:0110727",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110727",
            "name": "neuronal ceroid lipofuscinosis 13 Kufs type",
            "description": ""
        },
        {
            "id": "MONDO:0014147",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014147",
            "name": "neuronal ceroid lipofuscinosis 13",
            "description": "Any neuronal ceroid lipofuscinosis in which the cause of the disease is a mutation in the CTSF gene."
        },
        {
            "id": "MONDO:0014147",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014147",
            "name": "CLN13",
            "description": ""
        },
        {
            "id": "MONDO:0014147",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014147",
            "name": "CTSF neuronal ceroid lipofuscinosis",
            "description": ""
        },
        {
            "id": "MONDO:0014147",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014147",
            "name": "ceroid lipofuscinosis, neuronal, 13 (Kufs type)",
            "description": ""
        },
        {
            "id": "MONDO:0014147",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014147",
            "name": "ceroid lipofuscinosis, neuronal, type 13",
            "description": ""
        },
        {
            "id": "MONDO:0014147",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014147",
            "name": "neuronal ceroid lipofuscinosis caused by mutation in CTSF",
            "description": ""
        },
        {
            "id": "MONDO:0014147",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014147",
            "name": "neuronal ceroid lipofuscinosis type 13",
            "description": ""
        },
        {
            "id": "MONDO:0014147",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014147",
            "name": "ceroid lipofuscinosis, neuronal, 13",
            "description": ""
        },
        {
            "id": "MIM:615362",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615362",
            "name": "Ceroid lipofuscinosis, neuronal, 13 (Kufs type)",
            "description": "Ceroid lipofuscinosis, neuronal, 13 (Kufs type)"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110727"
    ],
    "unlinked_id_list": []
}