{
  "id": 16605,
  "label": "hypoaldosteronism disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015900",
  "properties": {
    "xrefs": [
      "GARD:0020228",
      "MEDGEN:208996",
      "MESH:D006994",
      "NANDO:2100132",
      "Orphanet:181419",
      "SCTID:60086000",
      "UMLS:C0857899"
    ],
    "synonyms": [
      "rare hypoaldosteronism",
      "hypoaldosteronism"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 7151,
      "label": "adrenal gland disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6875
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9553",
          "EFO:0005539",
          "ICD9:255",
          "ICD9:255.8",
          "ICD9:255.9",
          "MEDGEN:892577",
          "MESH:D000307",
          "NCIT:C26690",
          "SCTID:30171000",
          "UMLS:C4021794"
        ],
        "synonyms": [
          "adrenal gland disease",
          "adrenal gland disease or disorder",
          "adrenal gland diseases",
          "adrenal gland disorder",
          "adrenal gland disorders",
          "disease of adrenal gland",
          "disease or disorder of adrenal gland",
          "disorder of adrenal gland"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A disease involving the adrenal gland."
      },
      "child_count": 18,
      "reference_id": "MONDO:0005495"
    }
  ],
  "children": [
    {
      "id": 18558,
      "label": "familial hypoaldosteronism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16605
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016532",
          "MEDGEN:899592",
          "Orphanet:427",
          "SCTID:715343000",
          "UMLS:C4275180",
          "icd11.foundation:712299654"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Aldosterone synthase deficiency is a rare inherited defect of the final step of aldosterone biosynthesis (conversion of deoxycorticosterone to aldosterone)."
      },
      "child_count": 5,
      "reference_id": "MONDO:0018541"
    }
  ],
  "roots": [
    {
      "id": 7151,
      "label": "adrenal gland disorder"
    }
  ]
}