{
  "id": 2944,
  "label": "craniofacial dystonia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000486",
  "properties": {
    "xrefs": [
      "DOID:0050845",
      "GARD:0027532",
      "MEDGEN:868612",
      "UMLS:C4023011"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A focal dystonia that is characterized as dystonia that affects the muscles of the head, face, and neck."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "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"
    }
  ],
  "children": [
    {
      "id": 9253,
      "label": "lymphatic malformation 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2944,
        19154,
        23165,
        23452
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070213",
          "GARD:0003324",
          "MEDGEN:1648463",
          "MESH:C562467",
          "MedDRA:10027138",
          "OMIM:153200",
          "Orphanet:90186",
          "SCTID:400040008",
          "UMLS:C4746631"
        ],
        "synonyms": [
          "LMPH2",
          "Meige disease",
          "Meige lymphedema",
          "hereditary lymphedema type II",
          "late-onset primary lymphedema",
          "lymphedema hereditary type 2",
          "lymphedema praecox",
          "lymphedema, hereditary, II",
          "lymphedema, late-onset"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A frequent form of late-onset, primary lymphedema characterized by lower limb lymphedema typically developing during puberty."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007920"
    }
  ],
  "roots": [
    {
      "id": 2936,
      "label": "focal dystonia"
    }
  ]
}