{
  "id": 8601,
  "label": "bifid nose, autosomal dominant",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007195",
  "properties": {
    "xrefs": [
      "GARD:0015044",
      "MEDGEN:414016",
      "OMIM:109740",
      "UMLS:C2751431"
    ],
    "synonyms": [
      "bifid nose, autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0024623",
        "name": "otorhinolaryngologic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2727,
      "label": "bifid nose",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16263,
        21538
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000884",
          "MEDGEN:66379",
          "MESH:C535441",
          "Orphanet:2695",
          "UMLS:C0221363",
          "icd11.foundation:1824850646"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0024623",
            "name": "otorhinolaryngologic disease"
          }
        ],
        "definition": "Bifid nose is a rare congenital malformation of presumed autosomal dominant or recessive inheritance characterized by clefting of the nose ranging from a minimally noticeable groove in the columella to complete clefting of the underlying bones and cartilage (resulting in two half noses) with a usually adequate airway. Bifid nose may be seen in frontonasal dysplasia while other malformations such as hypertelorbitism and midline clefts of the lip may also be associated."
      },
      "child_count": 6,
      "reference_id": "MONDO:0000110"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2727,
      "label": "bifid nose"
    }
  ]
}