{
  "id": 16694,
  "label": "immunodeficiency with factor H anomaly",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016061",
  "properties": {
    "xrefs": [
      "GARD:0017099",
      "Orphanet:200421",
      "icd11.foundation:946399055"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 13404,
      "label": "complement factor H deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7021,
        18187
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018551",
          "ICD9:279.8",
          "MEDGEN:96024",
          "MESH:C562875",
          "NANDO:2200791",
          "OMIM:609814",
          "SCTID:234622003",
          "UMLS:C0398777"
        ],
        "synonyms": [
          "complement factor H deficiency",
          "CFHD",
          "Cfh deficiency",
          "factor H deficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0012350"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 13404,
      "label": "complement factor H deficiency"
    }
  ]
}