{
  "id": 9127,
  "label": "essential hypertension, genetic",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007781",
  "properties": {
    "xrefs": [
      "OMIM:145500"
    ],
    "synonyms": [
      "blood pressure regulation QTL",
      "genetic essential hypertension",
      "hypertension, essential, salt-sensitive",
      "hypertension, essential, susceptibility to, 2",
      "hypertension, essential, susceptibility to, 3",
      "hypertension, essential, susceptibility to, 4",
      "hypertension, essential, susceptibility to, 5",
      "hypertension, essential, susceptibility to, 6",
      "hypertension, susceptibility to",
      "EHT",
      "hypertension, essential",
      "hypertension, essential, susceptibility to",
      "hypertension, essential, susceptibility to, 1",
      "hypertension, salt-sensitive essential, susceptibility to"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "An instance of essential hypertension that is caused by a modification of the individual's genome."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3380,
      "label": "essential hypertension",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6776
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10825",
          "ICD9:401",
          "ICD9:401.9",
          "MEDGEN:88442",
          "MESH:D000075222",
          "Orphanet:243761",
          "SCTID:59621000",
          "UMLS:C0085580",
          "icd11.foundation:761947693"
        ],
        "synonyms": [
          "idiopathic hypertension",
          "primary hypertension"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Hypertension that presents without an identifiable cause."
      },
      "child_count": 3,
      "reference_id": "MONDO:0001134"
    },
    {
      "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": 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": 3380,
      "label": "essential hypertension"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 20011,
      "label": "inherited disease susceptibility"
    }
  ]
}