{
  "id": 24595,
  "label": "atypical dopamine transporter deficiency syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0700200",
  "properties": {
    "xrefs": [
      "DOID:0070488",
      "GARD:0026372"
    ],
    "synonyms": [
      "atypical DTDS"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A subset of SLC6A3-related DTDS cases which have later onset which ranges from late childhood to adulthood. This disorder is characterized by the presentation of parkinsonism-dystonia, rigidity, tremor, and bradykinesia after normal childhood development."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24512,
      "label": "SLC6A3-related dopamine transporter deficiency syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7073,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070487",
          "GARD:0026363"
        ],
        "synonyms": [
          "DTDS",
          "Dopamine transporter deficiency syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A complex movement disorder characterized by tremor, rigidity, bradykinesia, chorea, reduced facial expression, and Parkinsonism-dystonia. This disease is caused by loss of function variants in the SLC6A3 gene, which impair the dopamine transporter protein. The onset of this disease ranges from infancy to adulthood."
      },
      "child_count": 4,
      "reference_id": "MONDO:0700117"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24512,
      "label": "SLC6A3-related dopamine transporter deficiency syndrome"
    }
  ]
}