{
    "disease_id": "DOID:0070030", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007297", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "ADan amyloidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007297", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "dementia, familial Danish"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007297", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007297", 
            "name": "cerebellar ataxia, cataract, deafness, and dementia or psychosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007297", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007297", 
            "name": "FDD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007297", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007297", 
            "name": "Heredopathia Ophthalmootoencephalica"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007297", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007297", 
            "name": "cerebral amyloid angiopathy, ITM2B-RELATED, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007297", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007297", 
            "name": "cerebral amyloid angiopathy, ITM2B-related, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007297", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007297", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007297", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007297", 
            "name": "familial dementia, Danish type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007297", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007297", 
            "name": "HOOE"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070030", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070030", 
            "name": "FDD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070030", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070030", 
            "name": "Familial Danish Dementia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070030", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070030", 
            "name": "HOOE"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070030", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070030", 
            "name": "Heredopathia Ophthalmootoencephalica"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070030", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070030", 
            "name": "Cerebellar Ataxia, Cataract, Deafness, and Dementia Or Psychosis"
        }, 
        {
            "url": "https://www.omim.org/entry/117300", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:117300", 
            "name": "Cerebral amyloid angiopathy, ITM2B-related 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070030", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070030", 
        "name": "ITM2B-related cerebral amyloid angiopathy 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/117300", 
            "id": "117300", 
            "database": "MIM"
        }
    ]
}