{
  "id": 15252,
  "label": "episodic pain syndrome, familial, 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014246",
  "properties": {
    "xrefs": [
      "DOID:0111730",
      "GARD:0018440",
      "MEDGEN:816223",
      "OMIM:615551",
      "UMLS:C3809893"
    ],
    "synonyms": [
      "SCN10A familial episodic pain syndrome",
      "episodic pain syndrome, familial, 2",
      "episodic pain syndrome, familial, type 2",
      "familial episodic pain syndrome caused by mutation in SCN10A",
      "FEPS2"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any familial episodic pain syndrome in which the cause of the disease is a mutation in the SCN10A gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18414,
      "label": "familial episodic pain syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19748,
        20717
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111728",
          "GARD:0012684",
          "MEDGEN:1682682",
          "OMIMPS:615040",
          "Orphanet:391384",
          "UMLS:C5190598"
        ],
        "synonyms": [
          "FEPS"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0018319"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18414,
      "label": "familial episodic pain syndrome"
    }
  ]
}