{
  "id": 8881,
  "label": "dystonia 12",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007496",
  "properties": {
    "xrefs": [
      "DOID:0090056",
      "GARD:0009628",
      "MEDGEN:358384",
      "MESH:C538001",
      "NANDO:1200523",
      "NANDO:1200524",
      "NCIT:C157577",
      "OMIM:128235",
      "Orphanet:71517",
      "SCTID:702323008",
      "UMLS:C1868681"
    ],
    "synonyms": [
      "ATP1A3 dystonic disorder",
      "DYT-ATP1A3",
      "DYT12",
      "dystonia 12",
      "dystonia type 12",
      "dystonia-12",
      "dystonic disorder caused by mutation in ATP1A3",
      "RDP",
      "dystonia-Parkinsonism, rapid-onset",
      "rapid-onset dystonia-parkinsonism"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Rapid-onset dystonia-parkinsonism (RDP) is a very rare movement disorder, characterized by the abrupt onset of parkinsonism and dystonia, often triggered by physical or psychological stress."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19719,
      "label": "combined dystonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23452
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019432",
          "MEDGEN:1842879",
          "Orphanet:98203",
          "UMLS:C5680244"
        ],
        "synonyms": [
          "dystonia-plus syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A dystonia that is combined with another movement disorder (e.g., myoclonus, parkinsonism)."
      },
      "child_count": 10,
      "reference_id": "MONDO:0020065"
    },
    {
      "id": 20335,
      "label": "parkinsonian disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5849
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080855",
          "MEDGEN:66079",
          "MESH:D020734",
          "UMLS:C0242422"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA."
      },
      "child_count": 21,
      "reference_id": "MONDO:0021095"
    },
    {
      "id": 24400,
      "label": "ATP1A3-associated neurological disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24270
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "ATP1A3 neurological disorder",
          "ATP1A3 related neurological disorder",
          "neurological disorder caused by mutation in ATP1A3"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any neurological disorder in which the cause of the disease is a mutation in the ATP1A3."
      },
      "child_count": 4,
      "reference_id": "MONDO:0700002"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19719,
      "label": "combined dystonia"
    },
    {
      "id": 20335,
      "label": "parkinsonian disorder"
    },
    {
      "id": 24400,
      "label": "ATP1A3-associated neurological disorder"
    }
  ]
}