{
  "id": 17531,
  "label": "adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017189",
  "properties": {
    "xrefs": [
      "GARD:0021056",
      "MEDGEN:907576",
      "Orphanet:276608",
      "SCTID:717044000",
      "UMLS:C4274082"
    ],
    "synonyms": [
      "NI-PHH"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Diazoxide-resistant hyperinsulism (DRH) is form of congenital isolated hyperinsulinism caused by an abnormal insulin production by b-cells in the pancreas that can be diffuse or focal and is characterized by an excessive/ uncontrolled insulin secretion (inappropriate for the level of glycemia), recurrent episodes of profound hypoglycemia and resistance to medical management with diazoxide"
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17524,
      "label": "familial hyperinsulinism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4302,
        7419
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021053",
          "MEDGEN:854723",
          "NANDO:2100143",
          "NANDO:2200399",
          "NCIT:C131425",
          "Orphanet:276525",
          "UMLS:C3888018"
        ],
        "synonyms": [
          "hyperinsulinemic hypoglycemia",
          "FHI",
          "HHI",
          "congenital hyperinsulinism",
          "familial hyperinsulinemic hypoglycemia",
          "hereditary hyperinsulinism (disease)",
          "hyperinsulinemia of infancy",
          "neonatal hyperinsulinism",
          "nesidioblastosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "An instance of hyperinsulinism (disease) that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 6,
      "reference_id": "MONDO:0017182"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17524,
      "label": "familial hyperinsulinism"
    }
  ]
}