{
  "id": 5367,
  "label": "dystonic disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0003441",
  "properties": {
    "xrefs": [
      "DOID:543",
      "GARD:0027640",
      "HP:0001332",
      "ICD10CM:G24",
      "ICD9:333.90",
      "MEDGEN:3940",
      "MESH:D020821",
      "NCIT:C34563",
      "SCTID:15802004",
      "UMLS:C0013421"
    ],
    "synonyms": [
      "dystonia",
      "dystonic disorder",
      "dystonia disorder",
      "dystonia disorders"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A movement disorder characterized by sustained or intermittent muscle contractions, resulting in abnormal movements and/or postures."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 8,
  "parents": [
    {
      "id": 3996,
      "label": "extrapyramidal and movement disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7073
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13839",
          "ICD10CM:G20-G26",
          "ICD9:333.90",
          "MEDGEN:852565",
          "UMLS:C0477355"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0001815"
    }
  ],
  "children": [
    {
      "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": 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": 2938,
      "label": "segmental dystonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5367
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050838",
          "GARD:0027528",
          "ICD9:333.89",
          "MEDGEN:744778",
          "SCTID:427945008",
          "UMLS:C1997740"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A dystonia that affects two or more adjacent parts of the body."
      },
      "child_count": 2,
      "reference_id": "MONDO:0000479"
    },
    {
      "id": 17914,
      "label": "hemidystonia-hemiatrophy syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5367
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021273",
          "MEDGEN:1386711",
          "Orphanet:306741",
          "UMLS:C4510649"
        ],
        "synonyms": [
          "HD-HA syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Hemidystonia-hemiatrophy (HD-HA) is a rare dystonia, usually caused by a static cerebral injury occurring at birth or during infancy, that is characterized by a combination of hemidystonia (HD), involving one half of the body, and hemiatrophy (HA) on the same side as the HD."
      },
      "child_count": 0,
      "reference_id": "MONDO:0017649"
    },
    {
      "id": 23266,
      "label": "nocturnal paroxysmal dystonia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5367,
        23833
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027970",
          "MEDGEN:95991",
          "MESH:D020183",
          "SCTID:230500006",
          "UMLS:C0393777"
        ],
        "synonyms": [
          "dystonia, hypnogenic paroxysmal",
          "dystonia, nocturnal paroxysmal",
          "dystonia, nocturnal, paroxysmal",
          "dystonia, sleep-related",
          "dystonias, hypnogenic paroxysmal",
          "dystonias, nocturnal paroxysmal",
          "dystonias, sleep-related",
          "hypnogenic paroxysmal dystonia",
          "hypnogenic paroxysmal dystonias",
          "nocturnal paroxysmal dystonias",
          "paroxysmal dystonia, hypnogenic",
          "paroxysmal dystonia, nocturnal",
          "paroxysmal dystonias, hypnogenic",
          "paroxysmal dystonias, nocturnal",
          "sleep related dystonia",
          "sleep-related dystonia",
          "sleep-related dystonias"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A parasomnia characterized by paroxysmal episodes of choreoathetotic, ballistic, dystonic movements, and semipurposeful activity. The episodes occur during non-rapid eye movement sleep and typically recur several times per night."
      },
      "child_count": 0,
      "reference_id": "MONDO:0043969"
    },
    {
      "id": 23452,
      "label": "inherited dystonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5367,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021630",
          "MEDGEN:1842468",
          "NANDO:1200511",
          "NCIT:C35527",
          "OMIMPS:128100",
          "Orphanet:391799",
          "UMLS:C5680022"
        ],
        "synonyms": [
          "familial dystonia",
          "hereditary dystonic disorder",
          "rare genetic dystonia",
          "rare genetic dystonic disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of dystonic disorder that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 48,
      "reference_id": "MONDO:0044807"
    },
    {
      "id": 23453,
      "label": "idiopathic torsion dystonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5367,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027976",
          "ICD9:333.6",
          "MEDGEN:1850109",
          "NCIT:C34564",
          "SCTID:22451001",
          "UMLS:C5848258"
        ],
        "synonyms": [
          "Idiopathic torsion dystonia",
          "idiopathic torsion dystonia",
          "primary torsion dystonia",
          "Schwalbe disease",
          "Ziehen-oppenheim disease",
          "dystonia deformans progressiva",
          "dystonia musculorum deformans"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Torsion dystonia for which no underlying cause has been identified."
      },
      "child_count": 4,
      "reference_id": "MONDO:0044811"
    },
    {
      "id": 23456,
      "label": "torsion dystonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5367
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027978",
          "MEDGEN:3941",
          "SCTID:431034009",
          "UMLS:C0013423"
        ],
        "synonyms": [
          "torsion dystonia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0044843"
    }
  ],
  "roots": [
    {
      "id": 3996,
      "label": "extrapyramidal and movement disease"
    }
  ]
}