{
  "id": 11072,
  "label": "isolated Pierre-Robin syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009869",
  "properties": {
    "xrefs": [
      "GARD:0004347",
      "MEDGEN:19310",
      "MESH:D010855",
      "NCIT:C85010",
      "NORD:1579",
      "OMIM:261800",
      "Orphanet:718",
      "SCTID:4602007",
      "UMLS:C0031900",
      "icd11.foundation:136361299"
    ],
    "synonyms": [
      "Pierre Robin Sequence",
      "isolated Pierre Robin sequence",
      "Pierre Robin syndrome skeletal dysplasia polydactyly",
      "glossoptosis, micrognathia, and cleft palate"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Pierre-Robin syndrome (or Pierre-Robin sequence) is characterized by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 7019,
      "label": "eye disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4171,
        21415
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1242",
          "DOID:5614",
          "EFO:0003966",
          "ICD9:360",
          "ICD9:360.29",
          "ICD9:360.89",
          "ICD9:360.9",
          "ICD9:379.8",
          "ICD9:379.90",
          "MEDGEN:5092",
          "MESH:D005128",
          "NCIT:C26767",
          "SCTID:371405004",
          "UMLS:C0015397"
        ],
        "synonyms": [
          "disease of eye",
          "disease of eyeball of camera-type eye",
          "disease or disorder of eyeball of camera-type eye",
          "disorder of eye",
          "disorder of eyeball of camera-type eye",
          "eye disease",
          "eye disorder",
          "eyeball of camera-type eye disease",
          "eyeball of camera-type eye disease or disorder",
          "globe disease",
          "disease of eyeball",
          "disorder of eye proper",
          "disorder of eyeball",
          "disorder of globe"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A non-neoplastic or neoplastic disorder that affects the eye. Representative examples include conjunctivitis, glaucoma, cataract, conjunctival squamous cell carcinoma, uveal melanoma, and retinoblastoma."
      },
      "child_count": 240,
      "reference_id": "MONDO:0005328"
    }
  ],
  "children": [
    {
      "id": 23157,
      "label": "radial defect robin sequence",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        11072
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004624",
          "MEDGEN:419346",
          "MESH:C536261",
          "UMLS:C2931143"
        ],
        "synonyms": [
          "Bruce Winship syndrome",
          "Bruce winship syndrome",
          "bilateral radial defects club foot deformity micrognathia and cleft palate",
          "bilateral radial defects, club foot deformity, micrognathia and cleft palate"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0043191"
    }
  ],
  "roots": [
    {
      "id": 7019,
      "label": "eye disorder"
    }
  ]
}