{
  "id": 15264,
  "label": "neuronopathy, distal hereditary motor, type 2D",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014259",
  "properties": {
    "xrefs": [
      "DOID:0111210",
      "GARD:0018265",
      "MEDGEN:854832",
      "OMIM:615575",
      "UMLS:C3888271"
    ],
    "synonyms": [
      "FBXO38 neuronopathy, distal hereditary motor",
      "neuronopathy, distal hereditary motor caused by mutation in FBXO38",
      "HMN 2D",
      "HMN2D",
      "neuronopathy, distal hereditary motor, type IID",
      "neuropathy, distal hereditary motor, type 2D",
      "spinal muscular atrophy, distal, autosomal dominant, calf-predominant"
    ],
    "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 FBXO38 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"
    }
  ]
}