{
  "id": 9869,
  "label": "inherited torticollis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008583",
  "properties": {
    "xrefs": [
      "GARD:0004908",
      "HP:0000473",
      "ICD9:723.5",
      "MEDGEN:11859",
      "MESH:C535425",
      "NCIT:C4811",
      "OMIM:189600",
      "SCTID:268240006",
      "SCTID:70070008",
      "UMLS:C0040485"
    ],
    "synonyms": [
      "congenital torticollis",
      "fibromatosis colli",
      "inherited torticollis (disease)",
      "torticollis",
      "congenital muscular torticollis",
      "congenital sternomastoid torticollis",
      "congenital wry neck",
      "congenital wryneck",
      "contracture of sternocleidomastoid muscle",
      "familial spasmodic torticollis",
      "familial torticollis",
      "torticollis, congenital",
      "torticollis, familial"
    ],
    "categories": [
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      }
    ],
    "definition": "A congenital benign lesion that occurs in the distal sternocleidomastoid muscle of infants. It is characterized by the presence of plump spindle cells, and collagenous stroma formation."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6765,
      "label": "fibromatosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0000497",
          "MEDGEN:8836",
          "NCIT:C3042",
          "SCTID:723976005",
          "UMLS:C0016048"
        ],
        "synonyms": [
          "fibromatosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A poorly circumscribed neoplasm arising from the soft tissues. It is characterized by the presence of spindle-shaped fibroblasts and an infiltrative growth pattern."
      },
      "child_count": 3,
      "reference_id": "MONDO:0005031"
    },
    {
      "id": 21247,
      "label": "hereditary disorder of connective tissue",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        5762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:473110",
          "NCIT:C97075",
          "SCTID:363045008",
          "UMLS:C0410787"
        ],
        "synonyms": [
          "Mendelian connective tissue disorder",
          "connective tissue hereditary disorder",
          "hereditary connective tissue disorder",
          "Hereditary Connective Tissue Disorder",
          "Inherited disorder of connective tissue",
          "inherited disorder of connective tissue"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "An inherited genetic disorder that affects the connective tissues. Representative examples include Ehlers-Danlos syndrome and Marfan syndrome."
      },
      "child_count": 176,
      "reference_id": "MONDO:0023603"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6765,
      "label": "fibromatosis"
    },
    {
      "id": 21247,
      "label": "hereditary disorder of connective tissue"
    }
  ]
}