{
    "disease_id": "DOID:0070029", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008306", 
            "name": "ABri amyloidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008306", 
            "name": "Bri amyloidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008306", 
            "name": "familial dementia, British type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008306", 
            "name": "FBD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008306", 
            "name": "dementia, familial British"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008306", 
            "name": "familial British dementia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008306", 
            "name": "cerebral amyloid angiopathy, British type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008306", 
            "name": "dementia familial British"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008306", 
            "name": "presenile dementia with spastic ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008306", 
            "name": "cerebral amyloid angiopathy, ITM2B-RELATED, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008306", 
            "name": "cerebral amyloid angiopathy, ITM2B-related, type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070029", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070029", 
            "name": "Cerebral Amyloid Angiopathy, British Type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070029", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070029", 
            "name": "FBD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070029", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070029", 
            "name": "Familial British Dementia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070029", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070029", 
            "name": "Presenile Dementia with Spastic Ataxia"
        }, 
        {
            "url": "https://www.omim.org/entry/176500", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:176500", 
            "name": "Cerebral amyloid angiopathy, ITM2B-related 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070029", 
        "description": "A cerebral amyloid angiopathy characterized by onset in the 4th to 6th decade of life, progressive mental deterioration, spasticity, muscular rigidity but no tremors, spontaneous movements or sensory changes that has_material_basis_in an autosomal dominant mutation of ITM2B on chromosome 13q14.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070029", 
        "name": "ITM2B-related cerebral amyloid angiopathy 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/176500", 
            "id": "176500", 
            "database": "MIM"
        }
    ]
}