{
  "id": 22922,
  "label": "Mills syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0035892",
  "properties": {
    "xrefs": [
      "GARD:0019250",
      "MEDGEN:1682801",
      "Orphanet:94091",
      "UMLS:C5191669"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A rare, acquired motor neuron disease characterized by a slowly progressive, unilateral, ascending or descending hemplegia, associated to unilateral or asymmetrical pyramidal signs and no sensory loss. It is a diagnosis of exclusion and contorversy exists regarding whether the presence of bulbar symptoms, sphincter disturbances, fasciculations or cognitive manifestations characterize the disease."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19750,
      "label": "acquired motor neuron disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19749
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019479",
          "MEDGEN:1842733",
          "Orphanet:98506",
          "UMLS:C5680367"
        ],
        "synonyms": [
          "acquired anterior horn cell disease",
          "acquired motor neuron disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of motor neuron disease that is acquired during the lifetime of the individual."
      },
      "child_count": 3,
      "reference_id": "MONDO:0020129"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19750,
      "label": "acquired motor neuron disease"
    }
  ]
}