{
  "id": 13043,
  "label": "ovarian hyperstimulation syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011972",
  "properties": {
    "xrefs": [
      "DOID:5425",
      "GARD:0016668",
      "ICD9:256.1",
      "MEDGEN:38966",
      "MESH:D016471",
      "MedDRA:10033266",
      "OMIM:608115",
      "Orphanet:64739",
      "SCTID:129635004",
      "UMLS:C0085083",
      "icd11.foundation:1216664013"
    ],
    "synonyms": [
      "OHSS",
      "ovarian hyperstimulation syndrome",
      "ovarian hyperstimulation syndrome, familial gestational spontaneous"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "A complication of ovulation induction in infertility treatment. It is graded by the severity of symptoms which include ovary enlargement, multiple ovarian follicles; ovarian cysts; ascites; and generalized edema. The full-blown syndrome may lead to renal failure, respiratory distress, and even death. Increased capillary permeability is caused by the vasoactive substances, such as vascular endothelial growth factors, secreted by the overly-stimulated ovaries."
  },
  "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": 7207,
      "label": "ovarian disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4375,
        4379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1100",
          "EFO:0005771",
          "MEDGEN:892314",
          "MESH:D010049",
          "NCIT:C26841",
          "SCTID:5552004",
          "UMLS:C4021818"
        ],
        "synonyms": [
          "disease of ovary",
          "disease or disorder of ovary",
          "disorder of ovary",
          "ovarian disease",
          "ovarian disorder",
          "ovary disease",
          "ovary disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A disease involving the ovary."
      },
      "child_count": 22,
      "reference_id": "MONDO:0005558"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 7207,
      "label": "ovarian disorder"
    }
  ]
}