{
  "id": 12798,
  "label": "specific language impairment 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011711",
  "properties": {
    "xrefs": [
      "MEDGEN:338273",
      "OMIM:606712",
      "UMLS:C1847605"
    ],
    "synonyms": [
      "SLI2",
      "specific language impairment 2",
      "specific language impairment QTL, 2",
      "specific language impairment quantitative trait locus on chromosome 19"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3105,
      "label": "specific language impairment",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6521,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060244",
          "EFO:1001510",
          "MEDGEN:627772",
          "OMIMPS:606711",
          "Orphanet:458713",
          "UMLS:C0454651",
          "icd11.foundation:862918022"
        ],
        "synonyms": [
          "language impairment (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A language disorder characterized by difficulty in language acquisition despite otherwise normal development and in the absence of any obvious explanatory factors."
      },
      "child_count": 10,
      "reference_id": "MONDO:0000724"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3105,
      "label": "specific language impairment"
    }
  ]
}