{
  "id": 23919,
  "label": "allergic rhinitis, susceptibility to",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100177",
  "properties": {
    "xrefs": [
      "MEDGEN:865977",
      "OMIM:607154",
      "UMLS:C4017540"
    ],
    "synonyms": [
      "allergic rhinitis, susceptibility to"
    ],
    "definition": "An inherited susceptibility or predisposition to developing allergic rhinitis."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20011,
      "label": "inherited disease susceptibility",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23063
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD10CM:Z15",
          "MEDGEN:1876499",
          "MESH:D020022",
          "UMLS:C1455997"
        ],
        "synonyms": [
          "hereditary disease susceptibility",
          "hereditary predisposition to disease",
          "genetic predisposition",
          "genetic predispositions",
          "genetic susceptibilities",
          "genetic susceptibility",
          "predisposition, genetic",
          "predispositions, genetic",
          "susceptibilities, genetic",
          "susceptibility, genetic"
        ],
        "definition": "A latent susceptibility to disease at the genetic level, which may be activated under certain conditions."
      },
      "child_count": 284,
      "reference_id": "MONDO:0020573"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 20011,
      "label": "inherited disease susceptibility"
    }
  ]
}