{
  "id": 9487,
  "label": "Paget disease of bone 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008176",
  "properties": {
    "xrefs": [
      "DOID:0081366",
      "GARD:0004191",
      "MEDGEN:895927",
      "OMIM:167250",
      "UMLS:C4085252"
    ],
    "synonyms": [
      "Paget disease of bone 3",
      "Paget disease of bone type 3",
      "PDB3",
      "Paget disease of bone, familial",
      "familial Paget disease of bone"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7062,
      "label": "bone Paget disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4308,
        5714,
        25070
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5408",
          "EFO:0004261",
          "ICD10CM:M88",
          "MEDGEN:10493",
          "NCIT:C3292",
          "OMIMPS:167250",
          "Orphanet:280110",
          "SCTID:2089002",
          "UMLS:C0029401"
        ],
        "synonyms": [
          "Paget disease of bone",
          "Paget's bone disease",
          "Paget's disease of bone",
          "Paget's disease of the bone",
          "Pagets disease (bone)",
          "bone Paget disease",
          "bone Paget's disease",
          "osseous Paget's disease",
          "osteitis deformans",
          "Paget's disease",
          "familial Paget's disease of bone"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A disease of bone that initially results in the excessive resorption of bone (by osteoclasts) followed by the replacement of normal bone marrow with vascular and fibrous tissue."
      },
      "child_count": 15,
      "reference_id": "MONDO:0005382"
    },
    {
      "id": 25050,
      "label": "SQSTM1-related multisystem proteinopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18954,
        20409
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026565"
        ],
        "synonyms": [
          "SQSTM1-related multisystem proteinopathy"
        ],
        "definition": "A group of disorders including Paget disease of bone (PBD), inclusion body myopathy (IBM), and less frequently frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). Phenotypic presentation and severity are highly variable, and individuals within the same family may present with different associated conditions."
      },
      "child_count": 6,
      "reference_id": "MONDO:0800464"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7062,
      "label": "bone Paget disease"
    },
    {
      "id": 25050,
      "label": "SQSTM1-related multisystem proteinopathy"
    }
  ]
}