{
    "disease_id": "DOID:0070029",
    "recommended_name": {
        "id": "DOID:0070029",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070029",
        "name": "ITM2B-related cerebral amyloid angiopathy 1",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0070029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070029",
            "name": "Cerebral Amyloid Angiopathy, British Type",
            "description": ""
        },
        {
            "id": "DOID:0070029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070029",
            "name": "FBD",
            "description": ""
        },
        {
            "id": "DOID:0070029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070029",
            "name": "Familial British Dementia",
            "description": ""
        },
        {
            "id": "DOID:0070029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070029",
            "name": "Presenile Dementia with Spastic Ataxia",
            "description": ""
        },
        {
            "id": "MONDO:0008306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008306",
            "name": "ABri amyloidosis",
            "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."
        },
        {
            "id": "MONDO:0008306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008306",
            "name": "ABri amyloidosis",
            "description": ""
        },
        {
            "id": "MONDO:0008306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008306",
            "name": "Bri amyloidosis",
            "description": ""
        },
        {
            "id": "MONDO:0008306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008306",
            "name": "familial dementia, British type",
            "description": ""
        },
        {
            "id": "MONDO:0008306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008306",
            "name": "FBD",
            "description": ""
        },
        {
            "id": "MONDO:0008306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008306",
            "name": "dementia, familial British",
            "description": ""
        },
        {
            "id": "MONDO:0008306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008306",
            "name": "ITM2B-related cerebral amyloid angiopathy 1",
            "description": ""
        },
        {
            "id": "MONDO:0008306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008306",
            "name": "familial British dementia",
            "description": ""
        },
        {
            "id": "MONDO:0008306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008306",
            "name": "cerebral amyloid angiopathy, British type",
            "description": ""
        },
        {
            "id": "MONDO:0008306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008306",
            "name": "dementia familial British",
            "description": ""
        },
        {
            "id": "MONDO:0008306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008306",
            "name": "presenile dementia with spastic ataxia",
            "description": ""
        },
        {
            "id": "MONDO:0008306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008306",
            "name": "cerebral amyloid angiopathy, ITM2B-RELATED, 1",
            "description": ""
        },
        {
            "id": "MONDO:0008306",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008306",
            "name": "cerebral amyloid angiopathy, ITM2B-related, type 1",
            "description": ""
        },
        {
            "id": "MIM:176500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/176500",
            "name": "Cerebral amyloid angiopathy, ITM2B-related 1",
            "description": "Cerebral amyloid angiopathy, ITM2B-related 1"
        }
    ]
}