{
  "id": 21989,
  "label": "leukoencephalopathy, hereditary diffuse, with spheroids 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0030634",
  "properties": {
    "xrefs": [
      "GARD:0027268",
      "MEDGEN:1794254",
      "OMIM:619661",
      "UMLS:C5562044"
    ],
    "synonyms": [
      "HDLS2",
      "leukoencephalopathy, hereditary diffuse, with spheroids 2",
      "leukoencephalopathy, hereditary diffuse, with spheroids, swedish IIA"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 22045,
      "label": "leukoencephalopathy, hereditary diffuse, with spheroids",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:777989",
          "OMIMPS:221820",
          "UMLS:C3711381"
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0030796"
    },
    {
      "id": 26554,
      "label": "AARS1-related leukoencephalopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18952
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027336"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any leukoencephalopathy in which the cause of the disease is a variant in the AARS1 gene."
      },
      "child_count": 3,
      "reference_id": "MONDO:1010132"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 22045,
      "label": "leukoencephalopathy, hereditary diffuse, with spheroids"
    },
    {
      "id": 26554,
      "label": "AARS1-related leukoencephalopathy"
    }
  ]
}