{
  "id": 12840,
  "label": "familial hyperreninemic hypoaldosteronism type 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011754",
  "properties": {
    "xrefs": [
      "GARD:0024822",
      "MEDGEN:335571",
      "MESH:C564638",
      "OMIM:606984",
      "Orphanet:99764",
      "UMLS:C1846990"
    ],
    "synonyms": [
      "FHHA2",
      "aldosterone synthase deficiency unrelated to CYP11B2",
      "aldosterone synthase deficiency unrelated to the aldosterone synthase gene",
      "hyperreninemic hypoaldosteronism, familial, type 2",
      "Fhha2",
      "hyperreninemic hypoaldosteronism, familial, 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18558,
      "label": "familial hypoaldosteronism"
    }
  ]
}