{
  "id": 22278,
  "label": "hyperparathyroidism, transient neonatal",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0032591",
  "properties": {
    "xrefs": [
      "GARD:0016304",
      "MEDGEN:722059",
      "OMIM:618188",
      "UMLS:C1300287"
    ],
    "synonyms": [
      "HRPTTN",
      "hyperparathyroidism, transient neonatal"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16765,
      "label": "hereditary hyperparathyroidism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3927,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020408",
          "MEDGEN:1843372",
          "OMIMPS:145000",
          "Orphanet:208596",
          "UMLS:C5680826"
        ],
        "synonyms": [
          "genetic hyperparathyroidism"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "An instance of hyperparathyroidism that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 4,
      "reference_id": "MONDO:0016166"
    },
    {
      "id": 24807,
      "label": "abnormal mineralization disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18360
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026430"
        ],
        "synonyms": [
          "disorder of bone mineralization",
          "osteomalacia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A skeletal dysplasia where osteoid becomes calcified."
      },
      "child_count": 18,
      "reference_id": "MONDO:0800096"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16765,
      "label": "hereditary hyperparathyroidism"
    },
    {
      "id": 24807,
      "label": "abnormal mineralization disorder"
    }
  ]
}