{
  "id": 20171,
  "label": "spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020770",
  "properties": {
    "xrefs": [
      "DOID:0070465",
      "GARD:0025244",
      "MEDGEN:1673607",
      "OMIM:618387",
      "UMLS:C5193070"
    ],
    "synonyms": [
      "SCAN3",
      "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY 3"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20172,
      "label": "spinocerebellar ataxia, autosomal recessive, with axonal neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16133,
        20416
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025245",
          "MEDGEN:337609",
          "OMIMPS:607250",
          "UMLS:C1846574"
        ],
        "synonyms": [
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        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0020771"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 20172,
      "label": "spinocerebellar ataxia, autosomal recessive, with axonal neuropathy"
    }
  ]
}