{
  "id": 12971,
  "label": "idiopathic hypereosinophilic syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011895",
  "properties": {
    "xrefs": [
      "GARD:0016625",
      "ICD10CM:D72.110",
      "MEDGEN:61525",
      "OMIM:607685",
      "Orphanet:3260",
      "SCTID:423294001",
      "UMLS:C0206141",
      "icd11.foundation:703101846"
    ],
    "synonyms": [
      "hypereosinophilic syndrome, idiopathic, resistant to imatinib, isolated cases, somatic mutation",
      "HES",
      "hypereosinophilic syndrome, idiopathic"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 6836,
      "label": "idiopathic cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6735,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0000767",
          "GARD:0024149",
          "MEDGEN:18634",
          "NCIT:C53654",
          "UMLS:C0033141"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disease of the heart muscle or myocardium proper whose cause is unknown."
      },
      "child_count": 4,
      "reference_id": "MONDO:0005110"
    },
    {
      "id": 16456,
      "label": "hypereosinophilic syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        16883,
        23489
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:999",
          "EFO:1001467",
          "GARD:0002804",
          "ICD10CM:D72.11",
          "ICD9:288.3",
          "ICDO:9964/3",
          "MEDGEN:280990",
          "MESH:D017681",
          "MedDRA:10048643",
          "NANDO:2200805",
          "NANDO:2200806",
          "NCIT:C27038",
          "Orphanet:168956",
          "SCTID:419455006",
          "UMLS:C1540912",
          "icd11.foundation:110429919"
        ],
        "synonyms": [
          "HES",
          "hypereosinophilic disease",
          "hypereosinophilic disorder",
          "hypereosinophilic syndrome",
          "eosinophilia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Hypereosinophilic syndrome (HES) constitutes a rare and heterogeneous group of disorders, defined as persistent and marked blood eosinophilia and/or tissue eosinophilia associated with a wide range of clinical manifestations reflecting eosinophil-induced tissue/organ damage."
      },
      "child_count": 24,
      "reference_id": "MONDO:0015691"
    },
    {
      "id": 16880,
      "label": "familial restrictive cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6919,
        6933
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020532",
          "ICD9:425.4",
          "MEDGEN:468561",
          "OMIMPS:115210",
          "Orphanet:217635",
          "SCTID:233878008",
          "UMLS:C0340429"
        ],
        "synonyms": [
          "hereditary restrictive cardiomyopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "An instance of restrictive cardiomyopathy that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 20,
      "reference_id": "MONDO:0016340"
    }
  ],
  "children": [
    {
      "id": 19004,
      "label": "idiopathic acute eosinophilic pneumonia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6566,
        12971,
        16617,
        20092
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9503",
          "GARD:0000519",
          "MEDGEN:1371970",
          "NCIT:C35301",
          "NORD:728",
          "Orphanet:724",
          "SCTID:64936001",
          "UMLS:C4518469",
          "icd11.foundation:1455309767"
        ],
        "synonyms": [
          "Acute Eosinophilic Pneumonia",
          "IAEP",
          "Loeffler syndrome",
          "Loffler syndrome",
          "Loffler's syndrome",
          "Löffler syndrome",
          "pulmonary infiltrates with eosinophilia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Idiopathic acute eosinophilic pneumonia (IAEP) is an eosinophilic pneumonia of undetermined etiology that is characterized by acute febrile hypoxic respiratory failure associated with diffuse radiographic infiltrates and pulmonary eosinophilia, but without concurring allergy or infection."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019122"
    }
  ],
  "roots": [
    {
      "id": 6836,
      "label": "idiopathic cardiomyopathy"
    },
    {
      "id": 16456,
      "label": "hypereosinophilic syndrome"
    },
    {
      "id": 16880,
      "label": "familial restrictive cardiomyopathy"
    }
  ]
}