{
    "disease_id": "DOID:0070028",
    "recommended_name": {
        "id": "DOID:0070028",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070028",
        "name": "APP-related cerebral amyloid angiopathy",
        "description": "A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of APP on chromosome 21q21.3."
    },
    "synonyms": [
        {
            "id": "DOID:0070028",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070028",
            "name": "Cerebral Amyloid Angiopathy, App-Related, Dutch Variant",
            "description": ""
        },
        {
            "id": "DOID:0070028",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070028",
            "name": "Cerebral Amyloid Angiopathy, App-Related, Flemish Variant",
            "description": ""
        },
        {
            "id": "DOID:0070028",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070028",
            "name": "Amyloidosis, Cerebroarterial, App-Related",
            "description": ""
        },
        {
            "id": "DOID:0070028",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070028",
            "name": "HCHWAD",
            "description": ""
        },
        {
            "id": "DOID:0070028",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070028",
            "name": "Cerebral Amyloid Angiopathy, App-Related, Arctic Variant",
            "description": ""
        },
        {
            "id": "DOID:0070028",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070028",
            "name": "Cerebral Amyloid Angiopathy, App-Related, Italian Variant",
            "description": ""
        },
        {
            "id": "DOID:0070028",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070028",
            "name": "Cerebral Amyloid Angiopathy, App-Related, Iowa Variant",
            "description": ""
        },
        {
            "id": "DOID:0070028",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070028",
            "name": "Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant",
            "description": ""
        },
        {
            "id": "MONDO:0011583",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011583",
            "name": "cerebral amyloid angiopathy, APP-related",
            "description": "A cerebral amyloid angiopathy that has material basis in an autosomal dominant mutation of APP on chromosome 21q21.3."
        },
        {
            "id": "MONDO:0011583",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011583",
            "name": "HCHWAD",
            "description": ""
        },
        {
            "id": "MONDO:0011583",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011583",
            "name": "amyloidosis, Cerebroarterial, APP-related",
            "description": ""
        },
        {
            "id": "MONDO:0011583",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011583",
            "name": "cerebral amyloid angiopathy, APP-related",
            "description": ""
        },
        {
            "id": "MONDO:0011583",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011583",
            "name": "cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants",
            "description": ""
        },
        {
            "id": "MIM:605714",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/605714",
            "name": "Cerebral amyloid angiopathy, APP-related",
            "description": "Cerebral amyloid angiopathy, APP-related"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070028"
    ],
    "unlinked_id_list": []
}