{
  "id": 13916,
  "label": "heparin cofactor 2 deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012876",
  "properties": {
    "xrefs": [
      "DOID:0111901",
      "GARD:0024895",
      "ICD9:286.3",
      "MEDGEN:96017",
      "MESH:C562865",
      "OMIM:612356",
      "SCTID:234468009",
      "UMLS:C0398626"
    ],
    "synonyms": [
      "heparin cofactor 2 deficiency",
      "thrombophilia 10 due to heparin cofactor II deficiency",
      "Hcf 2 deficiency",
      "Hcf2 deficiency",
      "heparin cofactor II deficiency",
      "thrombophilia due to heparin cofactor 2 deficiency"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23980,
      "label": "inherited thrombophilia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4413,
        20411
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026094",
          "MEDGEN:391721",
          "OMIMPS:188050",
          "UMLS:C2584620"
        ],
        "synonyms": [
          "hereditary hypercoagulable disorder",
          "hereditary thrombophilia",
          "thrombophilia, hereditary"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "An instance of thrombophilia that is inherited."
      },
      "child_count": 24,
      "reference_id": "MONDO:0100240"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23980,
      "label": "inherited thrombophilia"
    }
  ]
}