{
  "id": 8739,
  "label": "cluster headache, familial",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007344",
  "properties": {
    "xrefs": [
      "GARD:0024553",
      "MEDGEN:350040",
      "MESH:C566117",
      "OMIM:119915",
      "UMLS:C1861513"
    ],
    "synonyms": [
      "cluster headache, familial",
      "hereditary cluster headache syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An instance of cluster headache syndrome that is caused by an inherited modification of the individual's genome."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23224,
      "label": "cluster headache syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7209,
        16344
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:3503",
          "MESH:D003027",
          "NCIT:C117077",
          "Orphanet:1002",
          "SCTID:193031009",
          "UMLS:C0009088",
          "icd11.foundation:760621151"
        ],
        "synonyms": [
          "Cephalgia, histamine",
          "Cephalgias, histamine",
          "Horton headache",
          "Horton syndrome",
          "Horton's headache",
          "Horton's neuralgia",
          "Horton's syndrome",
          "Hortons syndrome",
          "ciliary neuralgia",
          "ciliary neuralgias",
          "cluster headache",
          "cluster headache syndrome",
          "cluster migraine",
          "erythromelalgia of the head",
          "erythroprosopalgia of bing",
          "histamine cephalgia",
          "histamine cephalgias",
          "histamine headache",
          "migraine, neuralgic",
          "migraines, neuralgic",
          "migrainous neuralgia",
          "red migraine",
          "atypical cluster headache",
          "atypical cluster headaches",
          "beuralgias, ciliary",
          "chronic cluster headache",
          "chronic cluster headaches",
          "cluster headache syndromes",
          "cluster headache, atypical",
          "cluster headache, chronic",
          "cluster headache, episodic",
          "cluster headaches",
          "cluster headaches, atypical",
          "cluster headaches, chronic",
          "cluster headaches, episodic",
          "episodic cluster headache",
          "episodic cluster headaches",
          "headache syndrome, cluster",
          "headache syndromes, cluster",
          "headache, atypical cluster",
          "headache, chronic cluster",
          "headache, cluster",
          "headache, episodic cluster",
          "headaches, atypical cluster",
          "headaches, chronic cluster",
          "headaches, cluster",
          "headaches, episodic cluster",
          "neuralgia, ciliary",
          "neuralgic migraine",
          "neuralgic migraines",
          "syndrome, Horton",
          "syndrome, Horton's",
          "syndrome, cluster headache",
          "syndromes, cluster headache",
          "vasomotor headache"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A headache disorder that is characterized by periodic severe, unilateral orbital, supraorbital, and/or temporal pain, and is associated with ipsilateral cranial autonomic symptoms."
      },
      "child_count": 2,
      "reference_id": "MONDO:0043537"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23224,
      "label": "cluster headache syndrome"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}