{
  "id": 4358,
  "label": "factor XIII deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0002241",
  "properties": {
    "xrefs": [
      "GARD:0023095",
      "MEDGEN:1385982",
      "MESH:D005177",
      "NANDO:2200681",
      "UMLS:C4316906"
    ],
    "synonyms": [
      "FXIIID"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "An acquired or inherited coagulation disorder due to reduced levels and activity of factor XIII."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 4359,
      "label": "coagulation protein disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3738
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2212",
          "GARD:0023096",
          "MEDGEN:108723",
          "MESH:D020147",
          "NCIT:C27215",
          "SCTID:86075001",
          "UMLS:C0600503"
        ],
        "synonyms": [
          "coagulation factor deficiency",
          "coagulation factor deficiency syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Congenital or acquired deficiency of one of the coagulation factors. It results in bleeding."
      },
      "child_count": 28,
      "reference_id": "MONDO:0002242"
    }
  ],
  "children": [
    {
      "id": 18203,
      "label": "congenital factor XIII deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4358,
        4360,
        10564
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2211",
          "GARD:0010766",
          "ICD9:286.3",
          "MEDGEN:4639",
          "NANDO:2200681",
          "NCIT:C131633",
          "Orphanet:331",
          "SCTID:50189006",
          "UMLS:C0015530"
        ],
        "synonyms": [
          "fibrin-stabilizing factor deficiency",
          "factor XIII deficiency",
          "fibrin stabilising factor deficiency",
          "fibrin stabilizing factor deficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Congenital factor XIII deficiency is an inherited bleeding disorder due to reduced levels and activity of factor XIII (FXIII) and characterized by hemorrhagic diathesis frequently associated with spontaneous abortions and defective wound healing. Factor XIII deficiency is one of the most rare coagulation factor deficiencies."
      },
      "child_count": 6,
      "reference_id": "MONDO:0018029"
    },
    {
      "id": 20371,
      "label": "acquired factor XIII deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4358,
        20034
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022412",
          "MEDGEN:1393253",
          "NANDO:1200897",
          "NCIT:C131629",
          "Orphanet:599513",
          "UMLS:C0238120",
          "icd11.foundation:939366157"
        ],
        "synonyms": [
          "aFXIII",
          "acquired factor XIII deficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "An acquired coagulation disorder due to reduced levels and activity of factor XIII."
      },
      "child_count": 0,
      "reference_id": "MONDO:0021133"
    }
  ],
  "roots": [
    {
      "id": 4359,
      "label": "coagulation protein disease"
    }
  ]
}