{
  "id": 26351,
  "label": "brain small vessel disease 6 with leukoencephalopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0980711",
  "properties": {
    "xrefs": [
      "DOID:0061236",
      "OMIM:621394"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19950,
      "label": "familial porencephaly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        12183,
        17717,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112313",
          "GARD:0002258",
          "MEDGEN:401353",
          "OMIMPS:175780",
          "Orphanet:99810",
          "UMLS:C1867983",
          "icd11.foundation:1833583032"
        ],
        "synonyms": [
          "hereditary porencephaly",
          "familial porencephalic white matter disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of porencephaly that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 21,
      "reference_id": "MONDO:0020496"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19950,
      "label": "familial porencephaly"
    }
  ]
}