{
  "id": 19076,
  "label": "DEND syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019207",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 23906,
      "label": "permanent neonatal diabetes mellitus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16920,
        17928
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060639",
          "GARD:0010457",
          "MEDGEN:371484",
          "MESH:C563425",
          "NCIT:C114902",
          "OMIMPS:606176",
          "Orphanet:99885",
          "SCTID:609565001",
          "UMLS:C1833104",
          "icd11.foundation:33655955"
        ],
        "synonyms": [
          "PNDM",
          "monogenic diabetes of infancy",
          "developmental delay, epilepsy, and neonatal diabetes",
          "diabetes mellitus, permanent neonatal",
          "diabetes mellitus, permanent neonatal, with neurologic features",
          "diabetes mellitus, permanent, of infancy"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Permanent neonatal diabetes mellitus (PNDM) is a monogenic form of neonatal diabetes (NDM) characterized by persistent hyperglycemia within the first 12 months of life in general, requiring continuous insulin treatment."
      },
      "child_count": 10,
      "reference_id": "MONDO:0100164"
    }
  ],
  "children": [
    {
      "id": 20008,
      "label": "intermediate DEND syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19076
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019724",
          "MEDGEN:1843317",
          "Orphanet:99989",
          "UMLS:C5680423"
        ],
        "synonyms": [
          "developmental delay-epilepsy-neonatal diabetes syndrome, intermediate form"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Intermediate DEND syndrome (iDEND) is a rare mild form of DEND syndrome, a neonatal diabetes mellitus, developmental delay and epilepsy condition. The intermediate form is characterized clinically by mild motor, speech or cognitive delay and an absence of epilepsy."
      },
      "child_count": 0,
      "reference_id": "MONDO:0020569"
    },
    {
      "id": 24964,
      "label": "developmental delay, epilepsy, and neonatal diabetes 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19076
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026533",
          "MEDGEN:1709191",
          "UMLS:C5394597"
        ],
        "synonyms": [
          "DEND1"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0800375"
    },
    {
      "id": 24965,
      "label": "developmental delay, epilepsy, and neonatal diabetes 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19076
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0800376"
    }
  ],
  "roots": [
    {
      "id": 23906,
      "label": "permanent neonatal diabetes mellitus"
    }
  ]
}