{
  "id": 16642,
  "label": "familial isolated hypoparathyroidism due to impaired PTH secretion",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016000",
  "properties": {
    "xrefs": [
      "GARD:0017088",
      "MEDGEN:1843283",
      "Orphanet:189466",
      "UMLS:C5680524"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9141,
      "label": "hypoparathyroidism, familial isolated 1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16919
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061150",
          "GARD:0024578",
          "MEDGEN:1713884",
          "OMIM:146200",
          "SCTID:237657009",
          "UMLS:C5241444"
        ],
        "synonyms": [
          "FIH",
          "hypoparathyroidism, familial isolated",
          "FIH1",
          "hypoparathyroidism, familial isolated 1",
          "hypoparathyroidism familial isolated",
          "hypoparathyroidism, autosomal dominant",
          "hypoparathyroidism, autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0007796"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9141,
      "label": "hypoparathyroidism, familial isolated 1"
    }
  ]
}