{
  "id": 15956,
  "label": "myoclonus, intractable, neonatal",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014979",
  "properties": {
    "xrefs": [
      "MEDGEN:934625",
      "OMIM:617235",
      "UMLS:C4310658"
    ],
    "synonyms": [
      "NEIMY",
      "myoclonus, intractable, neonatal",
      "myoclonus, intractable, neonatal; NEIMY"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A severe neurologic disorder characterized by the onset of intractable myoclonic seizures soon after birth."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24348,
      "label": "KIF5A-related neurological disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24270
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "KIF5A-RD",
          "KIF5A-related disorder",
          "kinesin family member 5A (KIF5A)-related disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any nervous system disorder in which the cause of the disease is a variation in the KIF5A gene."
      },
      "child_count": 3,
      "reference_id": "MONDO:0100629"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24348,
      "label": "KIF5A-related neurological disorder"
    }
  ]
}