{
    "disease_id": "DOID:0061227",
    "recommended_name": {
        "id": "DOID:0061227",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061227",
        "name": "autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1",
        "description": "A CADASIL characterized by the onset of neurologic symptoms in infancy or early childhood that has_material_basis_in homozygous or compound heterozygous mutations in the NOTCH3 gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0979867",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0979867",
            "name": "cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1",
            "description": ""
        },
        {
            "id": "MIM:621295",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/621295",
            "name": "Cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1",
            "description": "Cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061227"
    ],
    "unlinked_id_list": []
}