{
  "id": 24047,
  "label": "sensory ataxia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100311",
  "properties": {
    "xrefs": [
      "MEDGEN:66020",
      "UMLS:C0240991"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any ataxia in which the causes of the disease is a perturbation of the sensory system, leading to its dysfunction."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 24044,
      "label": "atactic disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "ataxic disorder",
          "ataxia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A central nervous system disease that consists of gait impairment, unclear (“scanning”) speech, visual blurring due to nystagmus, hand incoordination, and tremor with movement."
      },
      "child_count": 4,
      "reference_id": "MONDO:0100308"
    }
  ],
  "children": [
    {
      "id": 13229,
      "label": "autosomal dominant sensory ataxia 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        24045,
        24047
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111170",
          "GARD:0024850",
          "MEDGEN:332346",
          "OMIM:608984",
          "UMLS:C1837015"
        ],
        "synonyms": [
          "ADSA",
          "RNF170 hereditary ataxia",
          "SNAX1",
          "hereditary ataxia caused by mutation in RNF170",
          "Adsa",
          "ataxia, sensory, 1, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any hereditary ataxia in which the cause of the disease is a mutation in the RNF170 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012166"
    },
    {
      "id": 24048,
      "label": "vestibular ataxia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        24047
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:863489",
          "UMLS:C4015052"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any ataxia in which the causes of the disease is a perturbation of the vestibular system, leading to its dysfunction."
      },
      "child_count": 0,
      "reference_id": "MONDO:0100312"
    }
  ],
  "roots": [
    {
      "id": 24044,
      "label": "atactic disorder"
    }
  ]
}