{
  "id": 9506,
  "label": "parietal foramina 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008197",
  "properties": {
    "xrefs": [
      "GARD:0018051",
      "MEDGEN:401480",
      "MESH:C566827",
      "OMIM:168500",
      "UMLS:C1868599"
    ],
    "synonyms": [
      "MSX2 parietal foramina",
      "parietal foramina 1",
      "parietal foramina caused by mutation in MSX2",
      "PFM",
      "PFM1",
      "catlin Marks",
      "cranium bifidum occultum",
      "cranium bifidum, hereditary",
      "foramina parietalia permagna",
      "parietal foramina",
      "parietal foramina, symmetric"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any parietal foramina in which the cause of the disease is a mutation in the MSX2 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18875,
      "label": "parietal foramina",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18236,
        18360,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060285",
          "GARD:0016662",
          "HP:0002697",
          "MESH:C566826",
          "OMIMPS:168500",
          "Orphanet:60015",
          "SCTID:718099006",
          "icd11.foundation:905361904"
        ],
        "synonyms": [
          "catlin marks",
          "enlarged parietal foramina",
          "fenestrae parietales symmetricae",
          "foramina parietalia permagna",
          "hereditary cranium bifidum",
          "parietal foramina",
          "symmetric parietal foramina"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Enlarged parietal foramina (EPF) is a developmental defect, characterized by variable intramembranous ossification defects of the parietal bones, which is either asymptomatic, symptomatic (headaches, nausea, vomiting, intellectual disability) or associated with other pathologies."
      },
      "child_count": 9,
      "reference_id": "MONDO:0018953"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18875,
      "label": "parietal foramina"
    }
  ]
}