{
  "id": 25217,
  "label": "autoimmune epilepsy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0850416",
  "properties": {
    "xrefs": [
      "DOID:0080994"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An epilepsy that is characterized by new-onset refractory seizures along with subacute progressive cognitive decline and behavioral or psychiatric dysfunction."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2996,
      "label": "autoimmune disorder of central nervous system",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4657,
        4981
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060004",
          "EFO:0020092"
        ],
        "synonyms": [
          "central nervous system autoimmune disease",
          "central nervous system hypersensitivity reaction type II disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A hypersensitivity reaction type II disease that involves the central nervous system."
      },
      "child_count": 16,
      "reference_id": "MONDO:0000568"
    },
    {
      "id": 23785,
      "label": "immune epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6761
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1371634",
          "UMLS:C4510729"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Epilepsies that have a distinct immune-mediated etiology with evidence of central nervous system inflammation, that has been demonstrated to be associated with a substantially increased risk of developing epilepsy."
      },
      "child_count": 2,
      "reference_id": "MONDO:0100028"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2996,
      "label": "autoimmune disorder of central nervous system"
    },
    {
      "id": 23785,
      "label": "immune epilepsy"
    }
  ]
}