{
    "disease_id": "DOID:0070030",
    "recommended_name": {
        "id": "DOID:0070030",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070030",
        "name": "ITM2B-related cerebral amyloid angiopathy 2",
        "description": "A cerebral amyloid angiopathy characterized by ataxia, intention tremor, psychosis and dementia that has_material_basis_in an autosomal dominant mutation of ITM2B on chromosome 13q14.2."
    },
    "synonyms": [
        {
            "id": "DOID:0070030",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070030",
            "name": "FDD",
            "description": ""
        },
        {
            "id": "DOID:0070030",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070030",
            "name": "Familial Danish Dementia",
            "description": ""
        },
        {
            "id": "DOID:0070030",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070030",
            "name": "HOOE",
            "description": ""
        },
        {
            "id": "DOID:0070030",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070030",
            "name": "Heredopathia Ophthalmootoencephalica",
            "description": ""
        },
        {
            "id": "DOID:0070030",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070030",
            "name": "Cerebellar Ataxia, Cataract, Deafness, and Dementia Or Psychosis",
            "description": ""
        },
        {
            "id": "MONDO:0007297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007297",
            "name": "ADan amyloidosis",
            "description": "A cerebral amyloid angiopathy characterized by ataxia, intention tremor, psychosis and dementia that has_material_basis_in an autosomal dominant mutation of ITM2B on chromosome 13q14.2."
        },
        {
            "id": "MONDO:0007297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007297",
            "name": "dementia, familial Danish",
            "description": ""
        },
        {
            "id": "MONDO:0007297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007297",
            "name": "ITM2B-related cerebral amyloid angiopathy 2",
            "description": ""
        },
        {
            "id": "MONDO:0007297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007297",
            "name": "cerebellar ataxia, cataract, deafness, and dementia or psychosis",
            "description": ""
        },
        {
            "id": "MONDO:0007297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007297",
            "name": "FDD",
            "description": ""
        },
        {
            "id": "MONDO:0007297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007297",
            "name": "Heredopathia Ophthalmootoencephalica",
            "description": ""
        },
        {
            "id": "MONDO:0007297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007297",
            "name": "cerebral amyloid angiopathy, ITM2B-RELATED, 2",
            "description": ""
        },
        {
            "id": "MONDO:0007297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007297",
            "name": "cerebral amyloid angiopathy, ITM2B-related, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007297",
            "name": "cerebellar ataxia, cataract, deafness, and dementia Or psychosis",
            "description": ""
        },
        {
            "id": "MONDO:0007297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007297",
            "name": "familial Danish dementia",
            "description": ""
        },
        {
            "id": "MONDO:0007297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007297",
            "name": "familial dementia, Danish type",
            "description": ""
        },
        {
            "id": "MONDO:0007297",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007297",
            "name": "HOOE",
            "description": ""
        },
        {
            "id": "MIM:117300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/117300",
            "name": "Cerebral amyloid angiopathy, ITM2B-related 2",
            "description": "Cerebral amyloid angiopathy, ITM2B-related 2"
        }
    ]
}