{
  "id": 10912,
  "label": "Unverricht-Lundborg syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009698",
  "properties": {
    "xrefs": [
      "DOID:0111452",
      "DOID:3535",
      "GARD:0003876",
      "MEDGEN:155923",
      "MESH:D020194",
      "MedDRA:10054895",
      "NANDO:1200954",
      "NANDO:2200880",
      "OMIM:254800",
      "Orphanet:308",
      "SCTID:230423006",
      "UMLS:C0751785"
    ],
    "synonyms": [
      "PME type 1",
      "ULD",
      "Unverricht-Lundborg disease",
      "Unverricht-Lundborg syndrome",
      "epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)",
      "progressive myoclonic epilepsy type 1",
      "progressive myoclonus epilepsy type 1",
      "Baltic myoclonic epilepsy",
      "EPM1",
      "Uld",
      "epilepsy, progressive myoclonic type 1",
      "epilepsy, progressive myoclonic, 1",
      "epilepsy, progressive myoclonic, 1A",
      "epilepsy, progressive myoclonus 1",
      "myoclonic epilepsy of Unverricht and Lundborg",
      "myoclonus progressive epilepsy of Unverricht and Lundborg",
      "progressive myoclonic epilepsy",
      "progressive myoclonus epilepsy Baltic myoclonic epilepsy"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Unverricht-Lundborg disease (ULD) is a rare progressive myoclonic epilepsy disorder characterized by action- and stimulus-sensitive myoclonus, and tonic-clonic seizures with ataxia, but with only a mild cognitive decline over time."
  },
  "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": 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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7073,
      "label": "movement disorder"
    },
    {
      "id": 19726,
      "label": "progressive myoclonus epilepsy"
    }
  ]
}