{
  "id": 17915,
  "label": "hyperekplexia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017658",
  "properties": {
    "xrefs": [
      "GARD:0021281",
      "MEDGEN:488800",
      "MESH:D000071017",
      "Orphanet:306773",
      "UMLS:C0234166"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A neurologic disorder classically characterized by pronounced startle responses to tactile or acoustic stimuli and hypertonia"
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "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"
    }
  ],
  "children": [
    {
      "id": 17916,
      "label": "sporadic hyperekplexia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17915
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021282",
          "MEDGEN:1683565",
          "Orphanet:306776",
          "UMLS:C5191042"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0017659"
    },
    {
      "id": 20273,
      "label": "hereditary hyperekplexia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17915,
        19114,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060695",
          "GARD:0003129",
          "MEDGEN:904633",
          "OMIMPS:149400",
          "Orphanet:3197",
          "SCTID:724351008",
          "UMLS:C4084968",
          "icd11.foundation:988250063"
        ],
        "synonyms": [
          "hyperekplexia",
          "Kok disease",
          "Stiff baby syndrome",
          "congenital stiff man syndrome",
          "familial startle disease",
          "hereditary hyperekplexia",
          "hereditary hyperexplexia",
          "hyperexplexia hereditary"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Hereditary hyperekplexia is a hereditary neurological disorder characterized by excessive startle responses."
      },
      "child_count": 15,
      "reference_id": "MONDO:0021022"
    }
  ],
  "roots": [
    {
      "id": 7073,
      "label": "movement disorder"
    }
  ]
}