{
  "id": 11887,
  "label": "X-linked dystonia-parkinsonism",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010747",
  "properties": {
    "xrefs": [
      "DOID:0090057",
      "GARD:0010533",
      "MEDGEN:326820",
      "MESH:C564048",
      "NANDO:1200514",
      "NCIT:C126330",
      "OMIM:314250",
      "Orphanet:53351",
      "SCTID:698279003",
      "UMLS:C1839130"
    ],
    "synonyms": [
      "DYT-TAF1",
      "DYT3",
      "Lubag",
      "Lubag syndrome",
      "X-linked dystonia Parkinsonism",
      "XDP",
      "dystonia-Parkinsonism, X-linked, X-linked recessive",
      "X-linked dystonia-Parkinsonism syndrome",
      "X-linked dystonia-parkinsonism/Lubag",
      "X-linked torsion dystonia-Parkinsonism syndrome",
      "dystonia 3, torsion, X-linked",
      "dystonia-Parkinsonism, X-linked",
      "torsion dystonia-Parkinsonism, Filipino type"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "X-linked dystonia-parkinsonism (XDP) is a neurodegenerative movement disorder characterized by adult-onset parkinsonism that is frequently accompanied by focal dystonia, which becomes generalized over time, and that has a highly variable clinical course."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2936,
      "label": "focal dystonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5367
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050836",
          "GARD:0027526",
          "MEDGEN:149279",
          "SCTID:445006008",
          "UMLS:C0743332"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A dystonia that is localized to a specific part of the body."
      },
      "child_count": 12,
      "reference_id": "MONDO:0000477"
    },
    {
      "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": 2936,
      "label": "focal dystonia"
    },
    {
      "id": 19719,
      "label": "combined dystonia"
    },
    {
      "id": 20335,
      "label": "parkinsonian disorder"
    }
  ]
}