{
    "disease_id": "DOID:0070027", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007098", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007098", 
            "name": "ACys amyloidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007098", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007098", 
            "name": "amyloidosis VI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007098", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007098", 
            "name": "HCHWA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007098", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007098", 
            "name": "cystatin amyloidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007098", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007098", 
            "name": "CST3-related amyloidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007098", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007098", 
            "name": "amyloidosis 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007098", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007098", 
            "name": "HCHWA, Icelandic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007098", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007098", 
            "name": "cerebral hemorrhage, hereditary, with amyloidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007098", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007098", 
            "name": "amyloidosis, Cerebroarterial, Icelandic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007098", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007098", 
            "name": "cerebral amyloid angiopathy, CST3-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007098", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007098", 
            "name": "hereditary cystatin C amyloid angiopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007098", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007098", 
            "name": "hereditary cerebral hemorrhage with amyloidosis, Icelandic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007098", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007098", 
            "name": "hereditary cerebral hemorrhage with amyloidosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070027", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070027", 
            "name": "Amyloidosis VI"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070027", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070027", 
            "name": "Amyloidosis, Cerebroarterial, Icelandic Type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070027", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070027", 
            "name": "HCHWA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070027", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070027", 
            "name": "Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070027", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070027", 
            "name": "Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant"
        }, 
        {
            "url": "https://www.omim.org/entry/105150", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:105150", 
            "name": "Amyloidosis 6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070027", 
        "description": "A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of CST3 on chromosome 20p11.21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070027", 
        "name": "CST3-related cerebral amyloid angiopathy"
    }, 
    "evidence": [
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            "url": "https://www.omim.org/entry/105150", 
            "id": "105150", 
            "database": "MIM"
        }
    ]
}