{
    "disease_id": "DOID:0111035",
    "recommended_name": {
        "id": "DOID:0111035",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111035",
        "name": "CADASIL 1",
        "description": "A CADASIL characterized by migraine, strokes, and white matter lesions that has_material_basis_in heterozygous mutation in the NOTCH3 gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "DOID:0111035",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111035",
            "name": "autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1",
            "description": "A CADASIL characterized by migraine, strokes, and white matter lesions that has material basis in heterozygous mutation in the NOTCH3 gene on chromosome 19p13."
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "CADASIL 1",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "CADASIL syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "CADASIL type 1",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "CADASIL1",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "dementia, hereditary multi-infarct type",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "hereditary multi-infarct dementia",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "CADASIL",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "CASIL",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "cerebral arteriopathy with subcortical infarcts and leukoencephalopathy",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "familial vascular leukoencephalopathy",
            "description": ""
        },
        {
            "id": "MIM:125310",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/125310",
            "name": "Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, 1",
            "description": "Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, 1"
        }
    ]
}