{
  "id": 16009,
  "label": "ABeta amyloidosis, dutch type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015033",
  "properties": {
    "xrefs": [
      "GARD:0016929",
      "ICD9:277.39",
      "MEDGEN:419468",
      "Orphanet:100006",
      "SCTID:56453003",
      "UMLS:C2931672",
      "icd11.foundation:1251572976"
    ],
    "synonyms": [
      "ABetaE22Q amyloidosis",
      "HCHWA, Dutch type",
      "HCHWA-D",
      "cerebral amyloid angiopathy, APP-related, Dutch variant",
      "hereditary cerebral haemorrhage with amyloidosis, Dutch type",
      "hereditary cerebral hemorrhage with amyloidosis, Dutch type"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Hereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA-D) is a form of HCHWA, a group of familial central nervous system disorders, characterized by severe cerebral amyloid angiopathy (CAA), hemorrhagic and non-hemorrhagic strokes and dementia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 12679,
      "label": "cerebral amyloid angiopathy, APP-related",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7260,
        29349
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070028",
          "GARD:0024810",
          "MEDGEN:414044",
          "NCIT:C157147",
          "OMIM:605714",
          "UMLS:C2751536"
        ],
        "synonyms": [
          "HCHWAD",
          "amyloidosis, Cerebroarterial, APP-related",
          "cerebral amyloid angiopathy, APP-related",
          "cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants",
          "APP-related cerebral amyloid angiopathy",
          "amyloidosis, hereditary, with cerebral hemorrhage, Dutch variant",
          "cerebral amyloid angiopathy, APP-related, Arctic variant",
          "cerebral amyloid angiopathy, APP-related, Dutch variant",
          "cerebral amyloid angiopathy, APP-related, Flemish variant",
          "cerebral amyloid angiopathy, APP-related, Iowa variant",
          "cerebral amyloid angiopathy, APP-related, Italian variant"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A cerebral amyloid angiopathy that has material basis in an autosomal dominant mutation of APP on chromosome 21q21.3."
      },
      "child_count": 12,
      "reference_id": "MONDO:0011583"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 12679,
      "label": "cerebral amyloid angiopathy, APP-related"
    }
  ]
}