{
  "id": 21511,
  "label": "febrile seizures, familial, 11",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0024566",
  "properties": {
    "xrefs": [
      "DOID:0111308",
      "GARD:0018283",
      "MEDGEN:482364",
      "OMIM:614418",
      "UMLS:C3280734"
    ],
    "synonyms": [
      "febrile seizures, familial, 11",
      "FEB11",
      "convulsions, familial febrile, 11"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2708,
      "label": "febrile seizures, familial",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111297",
          "OMIMPS:121210"
        ],
        "synonyms": [
          "seizures, familial febrile"
        ]
      },
      "child_count": 13,
      "reference_id": "MONDO:0000032"
    },
    {
      "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": 2708,
      "label": "febrile seizures, familial"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}