{
  "id": 17098,
  "label": "autosomal recessive ataxia due to PEX10 deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016614",
  "properties": {
    "xrefs": [
      "GARD:0020666",
      "MEDGEN:1843173",
      "Orphanet:247815",
      "UMLS:C5679614"
    ],
    "synonyms": [
      "mild peroxismal disorder due to PEX10 deficiency"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19712,
      "label": "autosomal recessive metabolic cerebellar ataxia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16133
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019413",
          "MEDGEN:1842756",
          "Orphanet:98096",
          "UMLS:C5681517"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 7,
      "reference_id": "MONDO:0020044"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19712,
      "label": "autosomal recessive metabolic cerebellar ataxia"
    }
  ]
}