{
  "id": 24965,
  "label": "developmental delay, epilepsy, and neonatal diabetes 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800376",
  "properties": {
    "xrefs": [
      "GARD:0026534",
      "MEDGEN:1712655",
      "UMLS:C5394304"
    ],
    "synonyms": [
      "DEND2"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19076,
      "label": "DEND syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23906
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016701",
          "MEDGEN:929262",
          "NCIT:C131845",
          "Orphanet:79134",
          "SCTID:721088003",
          "UMLS:C4303593"
        ],
        "synonyms": [
          "K ATP associated developmental delay, epilepsy and neonatal diabetes",
          "developmental delay-epilepsy-neonatal diabetes syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "DEND syndrome is a very rare, generally severe form of neonatal diabetes mellitus (NDM) characterized by a triad of developmental delay, epilepsy, and neonatal diabetes."
      },
      "child_count": 3,
      "reference_id": "MONDO:0019207"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19076,
      "label": "DEND syndrome"
    }
  ]
}