{
  "id": 10910,
  "label": "juvenile myoclonic epilepsy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009696",
  "properties": {
    "xrefs": [
      "DOID:4890",
      "GARD:0006808",
      "ICD10CM:G40.B",
      "ICD9:345.10",
      "MEDGEN:78738",
      "MESH:D020190",
      "MedDRA:10071082",
      "NCIT:C84796",
      "OMIM:254770",
      "OMIM:606904",
      "OMIMPS:254770",
      "Orphanet:307",
      "SCTID:6204001",
      "UMLS:C0270853",
      "icd11.foundation:1014397110"
    ],
    "synonyms": [
      "EJM",
      "JME",
      "epilepsy, myoclonic juvenile",
      "juvenile myoclonus epilepsy",
      "myoclonic epilepsy, juvenile",
      "myoclonic epilepsy, juvenile, 1",
      "myoclonic epilepsy, juvenile, susceptibility to, 1",
      "petit mal, impulsive"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "The most common hereditary idiopathic generalized epilepsy syndrome and is characterized by myoclonic jerks of the upper limbs on awakening, generalized tonic-clonic seizures manifesting during adolescence and triggered by sleep deprivation, alcohol intake, and cognitive activities, and typical absence seizures (30% of cases)."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 24301,
      "label": "myoclonic epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16436
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027276",
          "MEDGEN:4988",
          "UMLS:C0014550"
        ],
        "synonyms": [
          "myoclonic epilepsy syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A group of epilepsy syndromes in which myoclonic seizures are a prominent feature."
      },
      "child_count": 7,
      "reference_id": "MONDO:0100577"
    },
    {
      "id": 25071,
      "label": "variable-age onset idiopathic generalized epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7224,
        24339
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027390"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any idiopathic generalized epilepsy syndrome that has a variable-age onset."
      },
      "child_count": 8,
      "reference_id": "MONDO:0800487"
    }
  ],
  "children": [
    {
      "id": 24929,
      "label": "myoclonic epilepsy, juvenile, 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10910
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026505",
          "MEDGEN:854640",
          "UMLS:C3887932"
        ],
        "synonyms": [
          "EJM2"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0800330"
    }
  ],
  "roots": [
    {
      "id": 24301,
      "label": "myoclonic epilepsy"
    },
    {
      "id": 25071,
      "label": "variable-age onset idiopathic generalized epilepsy syndrome"
    }
  ]
}