{
  "id": 13146,
  "label": "neuronopathy, distal hereditary motor, type 2B",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012080",
  "properties": {
    "xrefs": [
      "DOID:0111207",
      "GARD:0018263",
      "MEDGEN:382017",
      "MESH:C567084",
      "OMIM:608634",
      "UMLS:C2608087"
    ],
    "synonyms": [
      "HSPB1 neuronopathy, distal hereditary motor",
      "neuronopathy, distal hereditary motor caused by mutation in HSPB1",
      "HMN 2B",
      "HMN2B",
      "neuronopathy, distal hereditary motor, type IIB",
      "neuropathy, distal hereditary motor, type 2B"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the HSPB1 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16214,
      "label": "distal hereditary motor neuropathy type 2",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16221
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111206",
          "GARD:0016954",
          "MEDGEN:777992",
          "MESH:C580044",
          "Orphanet:139525",
          "UMLS:C3711384",
          "icd11.foundation:152961055"
        ],
        "synonyms": [
          "dHMN2",
          "dSMA2",
          "distal spinal muscular atrophy type 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0015352"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16214,
      "label": "distal hereditary motor neuropathy type 2"
    }
  ]
}