{
  "id": 16661,
  "label": "Rasmussen subacute encephalitis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016019",
  "properties": {
    "xrefs": [
      "GARD:0018752",
      "ICD9:323.9",
      "MEDGEN:418934",
      "MESH:C535291",
      "NANDO:1200598",
      "NANDO:2100246",
      "NANDO:2200900",
      "NCIT:C125384",
      "NORD:1649",
      "Orphanet:1929",
      "SCTID:230191005",
      "UMLS:C2930868"
    ],
    "synonyms": [
      "CFE",
      "Rasmussen Encephalitis",
      "Rasmussen encephalitis",
      "Rasmussen syndrome",
      "Rasmussen’s encephalitis",
      "Rasmussen’s syndrome",
      "chronic focal encephalitis",
      "RE"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A rare, progressive chronic inflammation of a single cerebral hemisphere that usually affects children. It is characterized by severe seizures, loss of motor skills and speech, hemiparesis, and dementia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19722,
      "label": "postinfectious encephalitis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19721,
        20718
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10993",
          "GARD:0025152",
          "ICD9:323.6",
          "MEDGEN:581376",
          "MedDRA:10057235",
          "Orphanet:98253",
          "SCTID:192727001",
          "UMLS:C0393459"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 14,
      "reference_id": "MONDO:0020068"
    },
    {
      "id": 25079,
      "label": "variable-age epilepsy syndrome with developmental and/or epileptic encephalopathy or progressive neurological deterioration",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24339
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027300"
        ],
        "synonyms": [
          "VAE-SDE/PND"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An epilepsy syndrome characterized by seizures along with developmental and/or epileptic encephalopathy or progressive neurological deterioration where age at seizure onset varies."
      },
      "child_count": 2,
      "reference_id": "MONDO:0800495"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19722,
      "label": "postinfectious encephalitis"
    },
    {
      "id": 25079,
      "label": "variable-age epilepsy syndrome with developmental and/or epileptic encephalopathy or progressive neurological deterioration"
    }
  ]
}