{
  "id": 18851,
  "label": "SUNCT syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018927",
  "properties": {
    "xrefs": [
      "GARD:0009257",
      "MEDGEN:224724",
      "MESH:D050798",
      "MedDRA:10061981",
      "NCIT:C85174",
      "Orphanet:57145",
      "SCTID:725058003",
      "UMLS:C1262087"
    ],
    "synonyms": [
      "SUNCT headache",
      "short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing",
      "short-lasting, unilateral, neuralgiform headache attacks with conjunctival injection and tearing"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "SUNCT syndrome (Short-lasting Unilateral Neuralgiform headache attacks with Conjunctival injection and Tearing) is a primary headache disorder characterized by unilateral trigeminal pain that occurs in association with ipsilateral cranial autonomic symptoms (conjunctival injection and tearing)."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 16344,
      "label": "trigeminal autonomic cephalalgia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5448,
        17523,
        23165
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020017",
          "ICD9:339.09",
          "MEDGEN:327950",
          "MESH:D051303",
          "NCIT:C117074",
          "Orphanet:157843",
          "SCTID:449814007",
          "UMLS:C1565172",
          "icd11.foundation:607078588"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A headache disorder characterized by episodes of unilateral, short lasting pain and associated ipsilateral cranial autonomic symptoms."
      },
      "child_count": 12,
      "reference_id": "MONDO:0015530"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 16344,
      "label": "trigeminal autonomic cephalalgia"
    }
  ]
}