{
  "id": 20166,
  "label": "neuropathy, congenital hypomyelinating, 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020765",
  "properties": {
    "xrefs": [
      "GARD:0025242",
      "MEDGEN:1648446",
      "OMIM:618184",
      "UMLS:C4722277"
    ],
    "synonyms": [
      "CHN2",
      "NEUROPATHY, CONGENITAL HYPOMYELINATING, 2",
      "hypomyelinating neuropathy, congenital, 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 22641,
      "label": "neuropathy, congenital hypomelinating",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4427,
        19748
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025794",
          "MEDGEN:97965",
          "OMIMPS:605253",
          "UMLS:C0393818"
        ],
        "synonyms": [
          "CHN"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0033352"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 22641,
      "label": "neuropathy, congenital hypomelinating"
    }
  ]
}