{
    "disease_id": "DOID:13945",
    "recommended_name": {
        "id": "DOID:13945",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:13945",
        "name": "CADASIL",
        "description": "A leukodystrophy characterized by recurrent subcortical ischemic stroke and cognitive impairment."
    },
    "synonyms": [
        {
            "id": "DOID:13945",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13945",
            "name": "cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy",
            "description": ""
        },
        {
            "id": "DOID:13945",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13945",
            "name": "hereditary multi-infarct dementia",
            "description": ""
        },
        {
            "id": "MONDO:0010829",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010829",
            "name": "CARASIL",
            "description": "CARASIL is a hereditary cerebral small vessel disease characterized by early-onset gait disturbances, premature scalp alopecia, ischemic stroke, acute mid to lower back pain and progressive cognitive disturbances leading to severe dementia."
        },
        {
            "id": "MONDO:0010829",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010829",
            "name": "cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy",
            "description": ""
        },
        {
            "id": "MONDO:0010829",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010829",
            "name": "Maeda syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010829",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010829",
            "name": "cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy",
            "description": ""
        },
        {
            "id": "MONDO:0010829",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010829",
            "name": "CARASIL",
            "description": ""
        },
        {
            "id": "MONDO:0010829",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010829",
            "name": "cerebrovascular disease with thin skin, alopecia, and disc disease",
            "description": ""
        },
        {
            "id": "MONDO:0010829",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010829",
            "name": "cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy; CARASIL",
            "description": ""
        },
        {
            "id": "MONDO:0010829",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010829",
            "name": "subcortical vascular encephalopathy, progressive",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "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."
        },
        {
            "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": "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": "CADASIL 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": "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": "CADASIL1",
            "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; CADASIL1",
            "description": ""
        },
        {
            "id": "MONDO:0000914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0000914",
            "name": "CADASIL",
            "description": ""
        },
        {
            "id": "MIM:600142",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600142",
            "name": "Cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy",
            "description": "Cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy"
        },
        {
            "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"
        }
    ]
}