{
    "disease_id": "DOID:0070027",
    "recommended_name": {
        "id": "DOID:0070027",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070027",
        "name": "CST3-related cerebral amyloid angiopathy",
        "description": "A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of CST3 on chromosome 20p11.21."
    },
    "synonyms": [
        {
            "id": "DOID:0070027",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070027",
            "name": "Amyloidosis VI",
            "description": ""
        },
        {
            "id": "DOID:0070027",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070027",
            "name": "Amyloidosis, Cerebroarterial, Icelandic Type",
            "description": ""
        },
        {
            "id": "DOID:0070027",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070027",
            "name": "HCHWA",
            "description": ""
        },
        {
            "id": "DOID:0070027",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070027",
            "name": "Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant",
            "description": ""
        },
        {
            "id": "DOID:0070027",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070027",
            "name": "Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant",
            "description": ""
        },
        {
            "id": "MONDO:0007098",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007098",
            "name": "ACys amyloidosis",
            "description": "Hereditary cerebral hemorrhage with amyloidosis (HCHWA), Icelandic type is a form of HCHWA (see this term) characterized by an age of onset of 20-30 years, systemic amyloidosis and recurrent lobar intracerebral hemorrhages."
        },
        {
            "id": "MONDO:0007098",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007098",
            "name": "amyloidosis VI",
            "description": ""
        },
        {
            "id": "MONDO:0007098",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007098",
            "name": "HCHWA",
            "description": ""
        },
        {
            "id": "MONDO:0007098",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007098",
            "name": "cystatin amyloidosis",
            "description": ""
        },
        {
            "id": "MONDO:0007098",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007098",
            "name": "CST3-related amyloidosis",
            "description": ""
        },
        {
            "id": "MONDO:0007098",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007098",
            "name": "amyloidosis 6",
            "description": ""
        },
        {
            "id": "MONDO:0007098",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007098",
            "name": "HCHWA, Icelandic type",
            "description": ""
        },
        {
            "id": "MONDO:0007098",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007098",
            "name": "CST3-related cerebral amyloid angiopathy",
            "description": ""
        },
        {
            "id": "MONDO:0007098",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007098",
            "name": "cerebral hemorrhage, hereditary, with amyloidosis",
            "description": ""
        },
        {
            "id": "MONDO:0007098",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007098",
            "name": "amyloidosis, Cerebroarterial, Icelandic type",
            "description": ""
        },
        {
            "id": "MONDO:0007098",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007098",
            "name": "cerebral amyloid angiopathy, CST3-related",
            "description": ""
        },
        {
            "id": "MONDO:0007098",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007098",
            "name": "hereditary cystatin C amyloid angiopathy",
            "description": ""
        },
        {
            "id": "MONDO:0007098",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007098",
            "name": "hereditary cerebral hemorrhage with amyloidosis, Icelandic type",
            "description": ""
        },
        {
            "id": "MONDO:0007098",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007098",
            "name": "hereditary cerebral hemorrhage with amyloidosis",
            "description": ""
        },
        {
            "id": "MIM:105150",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/105150",
            "name": "Amyloidosis 6",
            "description": "Amyloidosis 6"
        }
    ]
}