{
  "id": 21188,
  "label": "inherited reflex epilepsy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0023224",
  "properties": {
    "synonyms": [
      "hereditary reflex epilepsy"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An instance of reflex epilepsy that is caused by an inherited modification of the individual's genome."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 17993,
      "label": "reflex epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6761
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2548",
          "EFO:1001146",
          "GARD:0018688",
          "ICD9:345.10",
          "MEDGEN:75726",
          "MESH:D020195",
          "NCIT:C85041",
          "Orphanet:310",
          "SCTID:79745005",
          "UMLS:C0270857",
          "icd11.foundation:276807111"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Reflex epilepsy refers to epilepsies where recurrent seizures are provoked by a clearly defined extrinsic (most commonly) or intrinsic triggering stimuli such as flashing lights (photosensitive epilepsy), startling noises (startle epilepsy), urinating (micturition induced seizures), exposure to hot-water (hot water epilepsy), eating, reading, and thinking, while being associated with an enduring abnormal predisposition to have such seizures (thereby meeting the conceptual definition of epilepsy)."
      },
      "child_count": 10,
      "reference_id": "MONDO:0017768"
    },
    {
      "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": [
    {
      "id": 14265,
      "label": "hot water reflex epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21188
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081104",
          "GARD:0017028",
          "ICD9:345.10",
          "MEDGEN:1631373",
          "OMIMPS:613339",
          "Orphanet:166412",
          "SCTID:230454005",
          "UMLS:C4706506"
        ],
        "synonyms": [
          "epilepsy, hot water",
          "hot water epilepsy",
          "bathing epilepsy",
          "water immersion epilepsy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Hot water reflex epilepsy is a rare neurologic disease characterized by the onset of generalized or focal seizures following immersion of the head in hot water, or with hot water being poured over the head. Primary generalized tonic-clonic seizures have been reported in rare cases."
      },
      "child_count": 2,
      "reference_id": "MONDO:0013229"
    },
    {
      "id": 16429,
      "label": "photosensitive epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21188,
        23212
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060281",
          "GARD:0005648",
          "ICD9:345.80",
          "MEDGEN:98285",
          "OMIMPS:132100",
          "Orphanet:166409",
          "SCTID:95208000",
          "UMLS:C0393720",
          "icd11.foundation:946957931"
        ],
        "synonyms": [
          "photoparoxysmal response",
          "PSE"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An epilepsy characterized by seizures triggered by visual stimuli that form patterns in space or time, such as flashing lights."
      },
      "child_count": 8,
      "reference_id": "MONDO:0015643"
    }
  ],
  "roots": [
    {
      "id": 17993,
      "label": "reflex epilepsy"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}