{
  "id": 17525,
  "label": "hyperinsulinism due to UCP2 deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017183",
  "properties": {
    "xrefs": [
      "GARD:0021054",
      "MEDGEN:928751",
      "Orphanet:276556",
      "SCTID:721834007",
      "UMLS:C4303082"
    ],
    "synonyms": [
      "hyperinsulinemic hypoglycemia due to UCP2 deficiency"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "HyHyperinsulism due to UCP2 deficiency (HIUCP2) is a form of diazoxide-sensitive diffuse hyperinsulinism (DHI) characterized by hypoglycemic episodes from the neonatal period, a good clinical response to diazoxide and a probable transient nature of the disease with spontaneous resolution."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16411,
      "label": "diazoxide-sensitive diffuse hyperinsulinism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18925
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020067",
          "MEDGEN:1842739",
          "Orphanet:165985",
          "UMLS:C5679570"
        ],
        "synonyms": [
          "hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 8,
      "reference_id": "MONDO:0015624"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16411,
      "label": "diazoxide-sensitive diffuse hyperinsulinism"
    }
  ]
}