{
  "id": 24291,
  "label": "myoclonic epilepsy in infancy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100566",
  "properties": {
    "xrefs": [
      "GARD:0019086",
      "MEDGEN:148242",
      "Orphanet:86909",
      "UMLS:C0751120"
    ],
    "synonyms": [
      "MEI",
      "benign myoclonic epilepsy of infancy",
      "benign myoclonus epilepsy of infancy"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A neonatal/infantile epilepsy syndrome that is characterized by the onset of myoclonic seizures between the ages of 6-18 months (range 4 months to 3 years). Males are twice as likely to be affected as females. Antecedent and birth history is unremarkable. Head size and neurological examination are normal. Prior development is usually normal. Cognitive, motor and behavioral difficulties are reported, especially if seizures are poorly controlled. Developmental outcome is normal in 60-85% of cases. Mild intellectual impairment and attention problems can be seen."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19724,
      "label": "infantile epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16436
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019436",
          "Orphanet:98258"
        ],
        "synonyms": [
          "epilepsy syndrome of infancy",
          "infantile epilepsy syndrome",
          "infantile onset epilepsy syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An epilepsy syndrome that occurs between 28 days to one year of life."
      },
      "child_count": 9,
      "reference_id": "MONDO:0020071"
    },
    {
      "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": 25072,
      "label": "neonatal/infantile-onset self-limited epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23780
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027296"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An epilepsy syndrome characterized by the onset of seizures in neonates/infants where there is a high likelihood of spontaneously remitting at a predictable age."
      },
      "child_count": 5,
      "reference_id": "MONDO:0800488"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19724,
      "label": "infantile epilepsy syndrome"
    },
    {
      "id": 24301,
      "label": "myoclonic epilepsy"
    },
    {
      "id": 25072,
      "label": "neonatal/infantile-onset self-limited epilepsy syndrome"
    }
  ]
}