{
  "id": 10473,
  "label": "fibrosclerosis, multifocal",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009230",
  "properties": {
    "xrefs": [
      "GARD:0005697",
      "ICD10CM:M35.5",
      "ICD9:710.8",
      "MEDGEN:105414",
      "MESH:C537375",
      "OMIM:228800",
      "SCTID:111210001",
      "UMLS:C0494949"
    ],
    "synonyms": [
      "fibrosclerosis, multifocal",
      "mediastinal fibrosis, familial",
      "multifocal fibrosclerosis",
      "retroperitoneal fibrosis, familial"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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"
    },
    {
      "id": 18784,
      "label": "IgG4-related retroperitoneal fibrosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17611
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009568",
          "ICD9:593.4",
          "MEDGEN:20554",
          "MESH:D012185",
          "MedDRA:10038979",
          "NCIT:C26876",
          "NORD:1665",
          "Orphanet:49041",
          "SCTID:197808006",
          "UMLS:C0035357",
          "icd11.foundation:900354709"
        ],
        "synonyms": [
          "Ormond disease",
          "Retroperitoneal Fibrosis",
          "idiopathic retroperitoneal fibrosis",
          "retroperitoneal fibrosis",
          "Ormond's disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Retroperitoneal fibrosis (RPF) is characterized by the development of a fibrotic mass surrounding retroperitoneal structures, such as aorta, vena cava, ureters and psoas muscle."
      },
      "child_count": 1,
      "reference_id": "MONDO:0018848"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 18784,
      "label": "IgG4-related retroperitoneal fibrosis"
    }
  ]
}