{
  "id": 26324,
  "label": "cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0979867",
  "properties": {
    "xrefs": [
      "DOID:0061227",
      "GARD:0028122",
      "OMIM:621295"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7611,
      "label": "autosomal recessive disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050737",
          "EFO:1000017",
          "ICD9:758.5",
          "MEDGEN:539209",
          "SCTID:85995004",
          "UMLS:C0265388"
        ],
        "synonyms": [
          "autosomal recessive disease or disorder",
          "autosomal recessive hereditary disease",
          "autosomal recessive hereditary disorder",
          "autosomal recessive inherited disease",
          "autosomal recessive inherited disorder",
          "disease or disorder, autosomal recessive",
          "disease, autosomal recessive",
          "recessive hereditary disorder (autosomal)"
        ],
        "definition": "Autosomal recessive form of disease."
      },
      "child_count": 219,
      "reference_id": "MONDO:0006025"
    },
    {
      "id": 8822,
      "label": "cerebral arteriopathy with subcortical infarcts and leukoencephalopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        5714,
        7065
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13945",
          "GARD:0024558",
          "ICD9:323.9",
          "ICD9:447.8",
          "MEDGEN:199687",
          "NANDO:1200545",
          "OMIMPS:125310",
          "UMLS:C0751587"
        ],
        "synonyms": [
          "CADASIL",
          "cerebral arteriopathy with subcortical infaracts and leukoencephalopathy",
          "cerebral arteriopathy with subcortical infarcts and leukoencephalopathy",
          "Casil",
          "cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy",
          "dementia, hereditary multi-infarct type"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 9,
      "reference_id": "MONDO:0007432"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7611,
      "label": "autosomal recessive disease"
    },
    {
      "id": 8822,
      "label": "cerebral arteriopathy with subcortical infarcts and leukoencephalopathy"
    }
  ]
}