{
  "id": 16134,
  "label": "opsoclonus-myoclonus syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015247",
  "properties": {
    "xrefs": [
      "EFO:1001383",
      "GARD:0010009",
      "ICD9:379.59",
      "MEDGEN:97955",
      "MESH:D053578",
      "MedDRA:10053854",
      "NCIT:C4686",
      "NORD:1527",
      "Orphanet:1183",
      "SCTID:230350000",
      "UMLS:C0393626"
    ],
    "synonyms": [
      "Ataxo-opso-myoclonus syndrome",
      "Kinsbourne syndrome",
      "OMS",
      "Opsoclonus-Myoclonus-Ataxia Syndrome",
      "POMA syndrome",
      "dancing eye syndrome",
      "dancing eye-dancing feet syndrome",
      "oma syndrome",
      "opsoclonus myoclonus syndrome",
      "opsoclonus-myoclonus-ataxia syndrome",
      "paraneoplastic opsoclonus-myoclonus",
      "paraneoplastic opsoclonus-myoclonus-ataxia syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Opsoclonus myoclonus syndrome (OMS) is a rare neuroinflammatory disease of paraneoplastic, parainfectious or idiopathic origin, characterized by opsoclonus, myoclonus, ataxia, and behavioral and sleep disorders."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7073,
      "label": "movement disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:480",
          "EFO:0004280",
          "ICD9:333.90",
          "ICD9:333.99",
          "MEDGEN:10113",
          "MESH:D009069",
          "NCIT:C116757",
          "SCTID:60342002",
          "UMLS:C0026650"
        ],
        "synonyms": [
          "movement disease",
          "movement disorder",
          "movement disorders"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Neurological conditions resulting in abnormal voluntary or involuntary movement, which may impact the speed, fluency, quality and ease of movement."
      },
      "child_count": 54,
      "reference_id": "MONDO:0005395"
    },
    {
      "id": 18348,
      "label": "paraneoplastic neurologic syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799,
        20314
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0007326",
          "ICD9:331.89",
          "MEDGEN:155656",
          "MedDRA:10072106",
          "Orphanet:36388",
          "SCTID:192877007",
          "UMLS:C0751911"
        ],
        "synonyms": [
          "PCD",
          "PNS",
          "nervous system paraneoplastic syndrome",
          "paraneoplastic syndrome of nervous system",
          "paraneoplastic cerebellar degeneration"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A paraneoplastic syndrome that involves the nervous system."
      },
      "child_count": 14,
      "reference_id": "MONDO:0018215"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7073,
      "label": "movement disorder"
    },
    {
      "id": 18348,
      "label": "paraneoplastic neurologic syndrome"
    }
  ]
}