{
  "id": 13829,
  "label": "dystonia 16",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012789",
  "properties": {
    "xrefs": [
      "DOID:0090048",
      "GARD:0010539",
      "MEDGEN:436979",
      "MESH:C567430",
      "NANDO:1200529",
      "NCIT:C168729",
      "OMIM:612067",
      "Orphanet:210571",
      "SCTID:722435003",
      "UMLS:C2677567",
      "icd11.foundation:548945828"
    ],
    "synonyms": [
      "DYT-PRKRA",
      "DYT16",
      "PRKRA dystonic disorder",
      "dystonia 16",
      "dystonia type 16",
      "dystonic disorder caused by mutation in PRKRA",
      "early-onset dystonia parkinsonism",
      "Young-onset dystonia-(parkinsonism)"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Dystonia 16 (DYT16) is a very rare and newly discovered movement disorder which is characterized by early-onset progressive limb dystonia, laryngeal and oromandibular dystonia, and parkinsonism."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2937,
      "label": "multifocal dystonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5367
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050837",
          "GARD:0027527"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A dystonia that involves two or more unrelated body parts."
      },
      "child_count": 3,
      "reference_id": "MONDO:0000478"
    },
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2937,
      "label": "multifocal dystonia"
    },
    {
      "id": 19719,
      "label": "combined dystonia"
    },
    {
      "id": 20335,
      "label": "parkinsonian disorder"
    }
  ]
}