{
    "disease_id": "DOID:0110731",
    "recommended_name": {
        "id": "DOID:0110731",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110731",
        "name": "neuronal ceroid lipofuscinosis 3",
        "description": "A neuronal ceroid lipofuscinosis that is characterized by juvenile-onset of progressive dementia, seizures, and progressive visual failure and an ultrastructural pattern of lipopigment with a 'fingerprint' profile and has_material_basis_in homozygous or compound heterozygous mutation in the CLN3 gene on chromosome 16p11."
    },
    "synonyms": [
        {
            "id": "DOID:0110731",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110731",
            "name": "Batten disease",
            "description": ""
        },
        {
            "id": "DOID:0110731",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110731",
            "name": "CLN3",
            "description": ""
        },
        {
            "id": "DOID:0110731",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110731",
            "name": "juvenile neuronal ceroid lipofuscinosis",
            "description": ""
        },
        {
            "id": "MONDO:0008767",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008767",
            "name": "neuronal ceroid lipofuscinosis 3",
            "description": "A condition associated with mutation(s) in the CLN3 gene, encoding battenin. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments."
        },
        {
            "id": "MONDO:0008767",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008767",
            "name": "CLN3",
            "description": ""
        },
        {
            "id": "MONDO:0008767",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008767",
            "name": "CLN3 neuronal ceroid lipofuscinosis",
            "description": ""
        },
        {
            "id": "MONDO:0008767",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008767",
            "name": "Juvenile CLN3 Disease",
            "description": ""
        },
        {
            "id": "MONDO:0008767",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008767",
            "name": "ceroid lipofuscinosis, neuronal, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0008767",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008767",
            "name": "neuronal ceroid lipofuscinosis 3",
            "description": ""
        },
        {
            "id": "MONDO:0008767",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008767",
            "name": "neuronal ceroid lipofuscinosis caused by mutation in CLN3",
            "description": ""
        },
        {
            "id": "MONDO:0008767",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008767",
            "name": "neuronal ceroid lipofuscinosis type 3",
            "description": ""
        },
        {
            "id": "MONDO:0008767",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008767",
            "name": "CLN3 disease, juvenile",
            "description": ""
        },
        {
            "id": "MONDO:0008767",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008767",
            "name": "Spielmeyer Sjogren disease",
            "description": ""
        },
        {
            "id": "MONDO:0008767",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008767",
            "name": "Vogt Spielmeyer disease",
            "description": ""
        },
        {
            "id": "MONDO:0008767",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008767",
            "name": "ceroid lipofuscinosis, neuronal, 3",
            "description": ""
        },
        {
            "id": "MIM:204200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/204200",
            "name": "Ceroid lipofuscinosis, neuronal, 3",
            "description": "Ceroid lipofuscinosis, neuronal, 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110731"
    ],
    "unlinked_id_list": []
}