{
  "id": 9207,
  "label": "familial congenital nasolacrimal duct obstruction",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007871",
  "properties": {
    "xrefs": [
      "GARD:0017784",
      "MEDGEN:332018",
      "MESH:C566703",
      "OMIM:149700",
      "Orphanet:451612",
      "UMLS:C1835612"
    ],
    "synonyms": [
      "LCDD",
      "lacrimal duct defect",
      "lacrimal puncta, absence of",
      "nasolacrimal duct obstruction"
    ],
    "categories": [
      {
        "ref": "MONDO:0024623",
        "name": "otorhinolaryngologic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18718,
      "label": "hereditary otorhinolaryngologic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        21538
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021935",
          "MEDGEN:1842579",
          "Orphanet:466084",
          "UMLS:C5681130"
        ],
        "synonyms": [
          "genetic otorhinolaryngologic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0024623",
            "name": "otorhinolaryngologic disease"
          }
        ],
        "definition": "An instance of otorhinolaryngologic disease that is caused by a modification of the individual's genome."
      },
      "child_count": 42,
      "reference_id": "MONDO:0018751"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18718,
      "label": "hereditary otorhinolaryngologic disease"
    }
  ]
}