{
  "id": 18461,
  "label": "epiphysiolysis of the hip",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018382",
  "properties": {
    "xrefs": [
      "GARD:0021666",
      "ICD10CM:M93.0",
      "MEDGEN:57704",
      "MESH:D060048",
      "OMIM:182260",
      "Orphanet:399329",
      "SCTID:26460006",
      "UMLS:C0149887"
    ],
    "synonyms": [
      "SCFE",
      "SUFE",
      "SufE",
      "epiphysiolysis capitis femoris",
      "epiphysiolysis of the upper femur",
      "femoral head epiphysiolysis",
      "slipped capital femoral epiphysis",
      "slipped femoral capital epiphyses",
      "slipped upper femoral epiphysis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Epiphysiolysis of the hip is a rare osteonecrosis disorder characterized by unilateral or bilateral disruption of the capital femoral physis with varying degrees of posterior epiphysis translation and simultaneous anterior metaphysis displacement. Patients typically present in pre-adolescence/adolescence with pain of variable intensity in varying locations (hip, groin, thigh, knee)."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18462,
      "label": "osteonecrosis of genetic origin",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        7060
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021667",
          "MEDGEN:1842788",
          "Orphanet:399380",
          "UMLS:C5680035"
        ],
        "synonyms": [
          "bone necrosis of genetic origin",
          "genetic osteonecrosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "An instance of osteonecrosis that is caused by a modification of the individual's genome."
      },
      "child_count": 24,
      "reference_id": "MONDO:0018383"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18462,
      "label": "osteonecrosis of genetic origin"
    }
  ]
}