{
  "id": 14792,
  "label": "trigonocephaly 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013774",
  "properties": {
    "xrefs": [
      "GARD:0018559",
      "MEDGEN:482604",
      "OMIM:614485",
      "UMLS:C3280974"
    ],
    "synonyms": [
      "FREM1 isolated trigonocephaly",
      "isolated trigonocephaly caused by mutation in FREM1",
      "trigonocephaly 2",
      "trigonocephaly type 2",
      "TRIGNO2",
      "craniosynostosis, metopic"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Any isolated trigonocephaly in which the cause of the disease is a mutation in the FREM1 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18228,
      "label": "isolated trigonocephaly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2748,
        16200
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016626",
          "MEDGEN:1812049",
          "NANDO:2201305",
          "OMIMPS:190440",
          "Orphanet:3366",
          "UMLS:C5575700"
        ],
        "synonyms": [
          "non-syndromic metopic craniosynostosis",
          "nonsyndromic trigonocephaly"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Isolated trigonocephaly is a nonsyndromic form of craniosynostosis characterized by the premature fusion of the metopic suture."
      },
      "child_count": 4,
      "reference_id": "MONDO:0018065"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18228,
      "label": "isolated trigonocephaly"
    }
  ]
}