{
  "id": 13229,
  "label": "autosomal dominant sensory ataxia 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012166",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24045,
      "label": "hereditary ataxia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24044,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050951",
          "EFO:0009671",
          "GARD:0020286",
          "ICD10CM:G11",
          "ICD10WHO:G11",
          "MEDGEN:2478",
          "MESH:C531684",
          "Orphanet:183518",
          "SCTID:763597000",
          "UMLS:C0004138",
          "icd11.foundation:442347652"
        ],
        "synonyms": [
          "rare hereditary ataxia",
          "SCA"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of an atactic disorder that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 40,
      "reference_id": "MONDO:0100309"
    },
    {
      "id": 24047,
      "label": "sensory ataxia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24044
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 2,
      "reference_id": "MONDO:0100311"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24045,
      "label": "hereditary ataxia"
    },
    {
      "id": 24047,
      "label": "sensory ataxia"
    }
  ]
}