{
  "id": 25079,
  "label": "variable-age epilepsy syndrome with developmental and/or epileptic encephalopathy or progressive neurological deterioration",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800495",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 24339,
      "label": "variable age epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16436
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027372",
          "Orphanet:699645"
        ],
        "synonyms": [
          "variable age onset epilepsy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An epilepsy syndrome that has an onset during variable ages and stages of life."
      },
      "child_count": 4,
      "reference_id": "MONDO:0100619"
    }
  ],
  "children": [
    {
      "id": 16661,
      "label": "Rasmussen subacute encephalitis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19722,
        25079
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0016019"
    },
    {
      "id": 19726,
      "label": "progressive myoclonus epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24270,
        24301,
        25079
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:891",
          "GARD:0007140",
          "MEDGEN:199732",
          "MESH:D020191",
          "NANDO:1200953",
          "NANDO:2100237",
          "NCIT:C7636",
          "NORD:1617",
          "OMIMPS:254800",
          "Orphanet:98261",
          "SCTID:267581004",
          "UMLS:C0751778",
          "icd11.foundation:173613583"
        ],
        "synonyms": [
          "PME",
          "epilepsy, progressive myoclonic",
          "progressive myoclonic epilepsy",
          "progressive myoclonic epilepsy (disorder) [ambiguous]",
          "progressive myoclonus epilepsy",
          "familial progressive myoclonic epilepsy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare group of disorders characterized by the development of myoclonic and tonic-clonic epileptic seizures associated with progressive degeneration of the nervous system."
      },
      "child_count": 45,
      "reference_id": "MONDO:0020074"
    }
  ],
  "roots": [
    {
      "id": 24339,
      "label": "variable age epilepsy syndrome"
    }
  ]
}