{
  "id": 12322,
  "label": "torsion dystonia 7",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011200",
  "properties": {
    "xrefs": [
      "DOID:0090040",
      "GARD:0007782",
      "MEDGEN:355560",
      "MESH:C566572",
      "NANDO:1200518",
      "OMIM:602124",
      "Orphanet:93963",
      "UMLS:C1865818"
    ],
    "synonyms": [
      "dystonia-7, torsion",
      "torsion dystonia type 7",
      "DYT7",
      "cervical dystonia, primary",
      "dystonia 7, torsion",
      "torsion dystonia, focal adult-onset"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A focal dystonia characterized by predominately cervical dystonia that has material basis in variation in the chromosome region 18p."
  },
  "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": 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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2936,
      "label": "focal dystonia"
    },
    {
      "id": 23452,
      "label": "inherited dystonia"
    }
  ]
}