{
    "disease_id": "DOID:0070028", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011583", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011583", 
            "name": "cerebral amyloid angiopathy, APP-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011583", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011583", 
            "name": "HCHWAD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011583", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011583", 
            "name": "amyloidosis, Cerebroarterial, APP-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011583", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011583", 
            "name": "cerebral amyloid angiopathy, APP-related, Dutch variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011583", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011583", 
            "name": "cerebral amyloid angiopathy, APP-related, Arctic variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011583", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011583", 
            "name": "amyloidosis, hereditary, with cerebral hemorrhage, Dutch variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011583", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011583", 
            "name": "cerebral amyloid angiopathy, APP-related, Italian variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011583", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011583", 
            "name": "cerebral amyloid angiopathy, APP-related, Iowa variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011583", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011583", 
            "name": "cerebral amyloid angiopathy, APP-related, Flemish variant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070028", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070028", 
            "name": "Cerebral Amyloid Angiopathy, App-Related, Dutch Variant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070028", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070028", 
            "name": "Cerebral Amyloid Angiopathy, App-Related, Flemish Variant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070028", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070028", 
            "name": "Amyloidosis, Cerebroarterial, App-Related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070028", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070028", 
            "name": "HCHWAD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070028", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070028", 
            "name": "Cerebral Amyloid Angiopathy, App-Related, Arctic Variant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070028", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070028", 
            "name": "Cerebral Amyloid Angiopathy, App-Related, Italian Variant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070028", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070028", 
            "name": "Cerebral Amyloid Angiopathy, App-Related, Iowa Variant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070028", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070028", 
            "name": "Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070028", 
        "description": "A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of APP on chromosome 21q21.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070028", 
        "name": "APP-related cerebral amyloid angiopathy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070028#disease-associations", 
            "id": "0070028", 
            "database": "Alliance of Genome Resources"
        }
    ]
}