{
  "id": 8511,
  "label": "ACys amyloidosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007098",
  "properties": {
    "xrefs": [
      "DOID:0070027",
      "GARD:0016930",
      "ICD9:277.39",
      "ICD9:437.8",
      "MEDGEN:279656",
      "OMIM:105150",
      "Orphanet:100008",
      "SCTID:703220002",
      "UMLS:C1527338",
      "icd11.foundation:1349991114"
    ],
    "synonyms": [
      "cerebral amyloid angiopathy",
      "CST3-related amyloidosis",
      "HCHWA, Icelandic type",
      "amyloidosis, Cerebroarterial, Icelandic type",
      "cerebral hemorrhage, hereditary, with amyloidosis",
      "cystatin amyloidosis",
      "hereditary cerebral haemorrhage with amyloidosis",
      "hereditary cerebral haemorrhage with amyloidosis, Icelandic type",
      "hereditary cerebral hemorrhage with amyloidosis",
      "hereditary cerebral hemorrhage with amyloidosis, Icelandic type",
      "hereditary cystatin C amyloid angiopathy",
      "CST3-related cerebral amyloid angiopathy",
      "amyloidosis 6",
      "cerebral amyloid angiopathy, CST3-related"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Hereditary cerebral hemorrhage with amyloidosis (HCHWA), Icelandic type is a form of HCHWA characterized by an age of onset of 20-30 years, systemic amyloidosis and recurrent lobar intracerebral hemorrhages."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7260,
      "label": "cerebral amyloid angiopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        12183,
        18631,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9246",
          "EFO:0006790",
          "GARD:0010266",
          "ICD10CM:I68.0",
          "ICD9:277.39",
          "MEDGEN:267610",
          "MESH:D016657",
          "NCIT:C84625",
          "Orphanet:85458",
          "SCTID:230724001",
          "UMLS:C1510489"
        ],
        "synonyms": [
          "HCHWA",
          "dutch hereditary cerebral amyloid angiopathy",
          "hereditary cerebral haemorrhage with amyloidosis - Dutch type",
          "hereditary cerebral hemorrhage with amyloidosis - Dutch type",
          "CAA, familial",
          "cerebral amyloid angiopathy, familial",
          "cerebral amyloid angiopathy, genetic"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Hereditary cerebral hemorrhage with amyloidosis (HCHWA) describes a group of rare familial central nervous system disorders characterized by amyloid deposition in the cerebral blood vessels leading to hemorrhagic and non-hemorrhagic strokes, focal neurological deficits, and progressive cognitive decline eventually leading to dementia."
      },
      "child_count": 12,
      "reference_id": "MONDO:0005620"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7260,
      "label": "cerebral amyloid angiopathy"
    }
  ]
}