{
  "id": 24338,
  "label": "VPS11-related neurological disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100617",
  "properties": {
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any neurological disorder in which the cause of the disease is a mutation in the VPS11 gene."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [
    {
      "id": 15724,
      "label": "hypomyelinating leukodystrophy 12",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18952,
        24338
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060796",
          "GARD:0017837",
          "MEDGEN:905068",
          "OMIM:616683",
          "Orphanet:466934",
          "UMLS:C4225247"
        ],
        "synonyms": [
          "HLD12",
          "VPS11 leukodystrophy",
          "VPS11-related autosomal recessive hypomyelinating leukoencephalopathy",
          "hypomyelinating leukodystrophy type 12",
          "leukodystrophy caused by mutation in VPS11",
          "leukodystrophy, hypomyelinating, 12",
          "leukodystrophy, hypomyelinating, type 12",
          "VPS11-related autosomal recessive hypomyelinating leukodystrophy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any leukodystrophy in which the cause of the disease is a mutation in the VPS11 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014732"
    },
    {
      "id": 21942,
      "label": "dystonia 32",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23452,
        24338
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060939",
          "GARD:0025578",
          "MEDGEN:1794239",
          "OMIM:619637",
          "UMLS:C5562029"
        ],
        "synonyms": [
          "DYT32"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030486"
    }
  ],
  "roots": [
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}