{
  "id": 10618,
  "label": "hyperlexia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009386",
  "properties": {
    "xrefs": [
      "MEDGEN:341011",
      "MESH:C565500",
      "OMIM:238350",
      "UMLS:C1855928"
    ],
    "synonyms": [
      "hyperlexia",
      "compulsive reading",
      "precocious reading"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3885,
      "label": "reading disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6464
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13365",
          "ICD9:315.00",
          "ICD9:315.09",
          "SCTID:52824009"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A learning disability involving difficulty reading resulting primarily from neurological factors which affect any part of the reading process."
      },
      "child_count": 3,
      "reference_id": "MONDO:0001697"
    },
    {
      "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": 3885,
      "label": "reading disorder"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}