{
    "disease_id": "DOID:0061189",
    "recommended_name": {
        "id": "DOID:0061189",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061189",
        "name": "neuronal ceroid lipofuscinosis 15",
        "description": "A neuronal ceroid lipofuscinosis that is characterized by severe global developmental delay apparent in infancy or early childhood and that has_material_basis_in heterozygous mutation in the CLCN6 gene on chromosome 1p36."
    },
    "synonyms": [
        {
            "id": "MONDO:0030947",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030947",
            "name": "neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities",
            "description": ""
        },
        {
            "id": "MONDO:0030947",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030947",
            "name": "CONRIBA",
            "description": ""
        },
        {
            "id": "MONDO:0030947",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030947",
            "name": "neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities",
            "description": ""
        },
        {
            "id": "MIM:619173",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619173",
            "name": "Ceroid lipofuscinosis, neuronal, 15",
            "description": "Ceroid lipofuscinosis, neuronal, 15"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061189"
    ],
    "unlinked_id_list": []
}