{
  "id": 9767,
  "label": "spondylolisthesis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008475",
  "properties": {
    "xrefs": [
      "DOID:6682",
      "EFO:0007493",
      "HP:0003302",
      "ICD10CM:M43.1",
      "MEDGEN:52470",
      "MESH:D013168",
      "NCIT:C35033",
      "OMIM:184200",
      "SCTID:274152003",
      "UMLS:C0038016",
      "icd11.foundation:1075039772"
    ],
    "synonyms": [
      "spondylolisthesis",
      "spondylolisthesis (disease)"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "A condition in which there is forward displacement of a vertebral bone over the on below it."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 3152,
      "label": "disease of bone structure",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7061
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080010",
          "MEDGEN:1843487",
          "UMLS:C0477681"
        ],
        "synonyms": [
          "bone structure disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0000836"
    },
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    }
  ],
  "children": [
    {
      "id": 21220,
      "label": "Jaffer-Beighton syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4370,
        9767
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:444079",
          "MESH:C537561",
          "UMLS:C2931533"
        ],
        "synonyms": [
          "Jaffer Beighton syndrome",
          "arachnodactyly, joint laxity, and spondylolisthesis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0023510"
    }
  ],
  "roots": [
    {
      "id": 3152,
      "label": "disease of bone structure"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    }
  ]
}