{
    "disease_id": "DOID:0111036", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014768", 
            "name": "cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014768", 
            "name": "CADASIL caused by mutation in HTRA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014768", 
            "name": "CADASIL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014768", 
            "name": "CADASIL type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014768", 
            "name": "autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014768", 
            "name": "HTRA1 CADASIL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014768", 
            "name": "cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2; CADASIL2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111036", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111036", 
            "name": "autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2"
        }, 
        {
            "url": "https://www.omim.org/entry/616779", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616779", 
            "name": "Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111036", 
        "description": "A CADASIL characterized by stroke, transient ischemic attacks, cognitive impairment, dementia, balance impairment, gait disturbance, headaches, and/or seizures associated with early confluent or confluent diffuse white matter hyperintensities that has_material_basis_in heterozygous mutation in the HTRA1 gene on chromosome 10q26.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111036", 
        "name": "CADASIL 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616779", 
            "id": "616779", 
            "database": "MIM"
        }
    ]
}