{
  "id": 18414,
  "label": "familial episodic pain syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018319",
  "properties": {
    "xrefs": [
      "DOID:0111728",
      "GARD:0012684",
      "MEDGEN:1682682",
      "OMIMPS:615040",
      "Orphanet:391384",
      "UMLS:C5190598"
    ],
    "synonyms": [
      "FEPS"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 19748,
      "label": "hereditary peripheral neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6950,
        24271
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010711",
          "MEDGEN:1825937",
          "Orphanet:98497",
          "UMLS:C5681733"
        ],
        "synonyms": [
          "genetic peripheral neuropathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of peripheral neuropathy that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 130,
      "reference_id": "MONDO:0020127"
    },
    {
      "id": 20717,
      "label": "neuralgia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6950,
        24453
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0009430",
          "ICD9:729.2",
          "MEDGEN:18010",
          "MESH:D009437",
          "SCTID:16269008",
          "UMLS:C0027796"
        ],
        "synonyms": [
          "neuralgia",
          "pain, nerve",
          "pain, neuropathic",
          "paroxysmal nerve pain",
          "paroxysmal nerve pains"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A pain disorder characterize by pain in the distribution of a nerve or nerves"
      },
      "child_count": 10,
      "reference_id": "MONDO:0021667"
    }
  ],
  "children": [
    {
      "id": 15031,
      "label": "familial episodic pain syndrome with predominantly upper body involvement",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18414
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111729",
          "GARD:0017618",
          "MEDGEN:814997",
          "OMIM:615040",
          "Orphanet:391389",
          "UMLS:C3808667"
        ],
        "synonyms": [
          "episodic pain syndrome, familial, type 1",
          "FEPS1",
          "episodic pain syndrome, familial, 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0014021"
    },
    {
      "id": 15252,
      "label": "episodic pain syndrome, familial, 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18414
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014246"
    },
    {
      "id": 15253,
      "label": "familial episodic pain syndrome with predominantly lower limb involvement",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4370,
        18414
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111731",
          "GARD:0017619",
          "MEDGEN:816229",
          "NCIT:C125390",
          "OMIM:615552",
          "Orphanet:391392",
          "UMLS:C3809899"
        ],
        "synonyms": [
          "episodic pain syndrome, familial, type 3",
          "FEPS3",
          "episodic pain syndrome, familial, 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare, autosomal dominant disorder caused by mutation in the SCN11A gene. It is characterized by intense episodic pain mainly affecting the distal lower extremities in early childhood. The pain diminishes with age."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014247"
    }
  ],
  "roots": [
    {
      "id": 19748,
      "label": "hereditary peripheral neuropathy"
    },
    {
      "id": 20717,
      "label": "neuralgia"
    }
  ]
}