{
  "id": 25080,
  "label": "epilepsy with auditory features",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800496",
  "properties": {
    "xrefs": [
      "GARD:0027394",
      "MEDGEN:1871199",
      "UMLS:C5967406"
    ],
    "synonyms": [
      "EAF"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A variable-age onset focal epilepsy syndrome with characteristic focal aware sensory auditory seizures. Seizures often produce such mild symptoms that they are not diagnosed. There are no implications expected for development or learning and seizures are typically infrequent and well controlled. EAF may occur as a familial syndrome, familial EAF (FEAF, previous known as autosomal dominant lateral temporal lobe epilepsy or autosomal dominant partial epilepsy with auditory features). Inheritance may be autosomal dominant (ADEAF), with incomplete penetrance."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 25076,
      "label": "variable-age onset focal epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7064,
        24339
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027391"
        ],
        "synonyms": [
          "VAOFAS"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An epilepsy syndrome characterized by focal seizures where age at seizure onset varies."
      },
      "child_count": 8,
      "reference_id": "MONDO:0800492"
    }
  ],
  "children": [
    {
      "id": 12031,
      "label": "autosomal dominant epilepsy with auditory features",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17942,
        25080
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0002257",
          "MEDGEN:325326",
          "MESH:C537297",
          "Orphanet:101046",
          "UMLS:C1838062",
          "icd11.foundation:832717248"
        ],
        "synonyms": [
          "ADEAF",
          "ADLTE",
          "ADPEAF",
          "Autosomal dominant epilepsy with auditory features",
          "adolescent/adult onset autosomal dominant epilepsy with auditory features",
          "autosomal dominant epilepsy with auditory features",
          "autosomal dominant lateral temporal lobe epilepsy",
          "autosomal dominant partial/lateral temporal epilepsy with auditory features",
          "partial epilepsy with auditory aura",
          "partial epilepsy with auditory features",
          "autosomal dominant partial epilepsy with auditory features"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare, genetic, familial partial epilepsy disease characterized by focal seizures associated with prominent ictal auditory symptoms, and/or receptive aphasia, presenting in two or more family members and having a relatively benign evolution."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010898"
    }
  ],
  "roots": [
    {
      "id": 25076,
      "label": "variable-age onset focal epilepsy syndrome"
    }
  ]
}