{
  "id": 14498,
  "label": "immunodeficiency due to ficolin3 deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013467",
  "properties": {
    "xrefs": [
      "GARD:0017513",
      "MEDGEN:462576",
      "NANDO:2200794",
      "OMIM:613860",
      "Orphanet:331190",
      "SCTID:766705006",
      "UMLS:C3151226"
    ],
    "synonyms": [
      "Fcn3 deficiency",
      "ficolin 3 deficiency",
      "immunodeficiency due to ficolin 3 deficiency",
      "lectin complement activation pathway, defect in, 3"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23298,
      "label": "disorder of lectin complement activation pathway",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5701
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025884",
          "OMIMPS:614372"
        ],
        "synonyms": [
          "complement activation, lectin pathway disease",
          "disorder of complement activation, lectin pathway"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A disease that has its basis in the disruption of complement activation, lectin pathway."
      },
      "child_count": 3,
      "reference_id": "MONDO:0044209"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23298,
      "label": "disorder of lectin complement activation pathway"
    }
  ]
}