{
  "id": 25621,
  "label": "developmental and epileptic encephalopathy, 31B",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0957248",
  "properties": {
    "xrefs": [
      "DOID:0070376",
      "GARD:0026796",
      "MEDGEN:1841095",
      "OMIM:620352",
      "UMLS:C5830459"
    ],
    "synonyms": [
      "DNM1-encephalopathy and neurodevelopmental disorder",
      "DEE31B",
      "developmental and epileptic encephalopathy 31B, autosomal recessive"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any developmental and epileptic encephalopathy in which the cause of the disease is a homozygous mutation in the DNM1 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24713,
      "label": "DNM1-encephalopathy and neurodevelopmental disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23814
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027295"
        ],
        "synonyms": [
          "DNM1-related DEE",
          "DNM1-related developmental and epileptic encephalopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A developmental and epileptic encephalopathy in which the cause of the disease is a variation in the DNM1 gene."
      },
      "child_count": 2,
      "reference_id": "MONDO:0700339"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24713,
      "label": "DNM1-encephalopathy and neurodevelopmental disorder"
    }
  ]
}