{
  "id": 9483,
  "label": "hypertrophic osteoarthropathy, primary, autosomal dominant",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008172",
  "properties": {
    "xrefs": [
      "GARD:0015101",
      "MEDGEN:382429",
      "OMIM:167100",
      "UMLS:C2674695"
    ],
    "synonyms": [
      "PHOAD",
      "hypertrophic osteoarthropathy, primary, autosomal dominant",
      "PDP, autosomal dominant",
      "Pho, autosomal dominant",
      "pachydermoperiostosis, autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4222,
      "label": "musculoskeletal system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:17",
          "EFO:0009676",
          "ICD9:729.99",
          "MEDGEN:6471",
          "MESH:D009140",
          "NCIT:C107377",
          "SCTID:928000",
          "UMLS:C0026857"
        ],
        "synonyms": [
          "disease of musculoskeletal system",
          "disease or disorder of musculoskeletal system",
          "disorder of musculoskeletal system",
          "musculoskeletal disease",
          "musculoskeletal system disease",
          "musculoskeletal system disease or disorder",
          "musculoskeletal system disorder",
          "musculoskeletal disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A disease involving the musculoskeletal system."
      },
      "child_count": 22,
      "reference_id": "MONDO:0002081"
    },
    {
      "id": 17104,
      "label": "primary hypertrophic osteoarthropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:14283",
          "GARD:0020667",
          "MEDGEN:18210",
          "MESH:D010004",
          "MedDRA:10051686",
          "NANDO:1200642",
          "NANDO:2100288",
          "NANDO:2201004",
          "NCIT:C85023",
          "OMIMPS:259100",
          "Orphanet:248095",
          "Orphanet:2796",
          "SCTID:88220006",
          "UMLS:C0029411",
          "icd11.foundation:792225761"
        ],
        "synonyms": [
          "PDP",
          "PHO",
          "Touraine Solente Gole syndrome",
          "Touraine-Solente-Gole syndrome",
          "hypertrophic osteoarthropathy, primary",
          "hypertrophic osteoarthropathy, primary, autosomal recessive, type 1",
          "hypertropic osteoarthropathy, primary",
          "idiopathic hypertrophic osteoarthropathy",
          "pachydermoperiostosis",
          "pachydermoperiostosis of nail [ambiguous]",
          "PHOAR1",
          "hypertrophic osteoarthropathy, primary, autosomal recessive, 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A genetically and clinically heterogeneous inherited disorder characterized by digital clubbing and osteoarthropathy, with variable features of pachydermia, delayed closure of the fontanels, and congenital heart disease. There are two types of PHO: pachydermoperiostosis and cranio-osteoarthropathy."
      },
      "child_count": 8,
      "reference_id": "MONDO:0016620"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4222,
      "label": "musculoskeletal system disorder"
    },
    {
      "id": 17104,
      "label": "primary hypertrophic osteoarthropathy"
    }
  ]
}