{
  "id": 14296,
  "label": "esophagitis, eosinophilic, 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013260",
  "properties": {
    "xrefs": [
      "GARD:0024909",
      "MEDGEN:462029",
      "OMIM:613412",
      "UMLS:C3150679"
    ],
    "synonyms": [
      "EOE2",
      "esophagitis, eosinophilic, 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 7044,
      "label": "eosinophilic esophagitis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3630,
        18486
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13922",
          "EFO:0004232",
          "GARD:0027720",
          "ICD10CM:K20.0",
          "ICD9:530.13",
          "MEDGEN:83318",
          "MESH:D057765",
          "MedDRA:10064212",
          "NANDO:1200456",
          "NCIT:C27105",
          "Orphanet:73247",
          "SCTID:235599003",
          "UMLS:C0341106"
        ],
        "synonyms": [
          "EoE"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "Eosinophilic esophagitis (EoE) is a chronic, allergic disease of the esophagus characterized clinically by symptoms of esophageal dysfunction (including vomiting, dysphagia, feeding disorders, food impaction and abdominal pain) which persist after treatment with proton pump inhibitors (PPIs)."
      },
      "child_count": 6,
      "reference_id": "MONDO:0005361"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 7044,
      "label": "eosinophilic esophagitis"
    }
  ]
}