{
  "id": 3105,
  "label": "specific language impairment",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000724",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "id": 6521,
      "label": "language disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4305
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:93",
          "HP:0002463",
          "MEDGEN:44069",
          "MESH:D007806",
          "NCIT:C97155",
          "UMLS:C0023015"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A category of disorders characterized by an impairment in the development of an individual's language capabilities, which is in contrast to his/her non-verbal intellect."
      },
      "child_count": 6,
      "reference_id": "MONDO:0004750"
    },
    {
      "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": 12797,
      "label": "specific language impairment 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3105
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:339804",
          "OMIM:606711",
          "UMLS:C1847614"
        ],
        "synonyms": [
          "SLI1",
          "specific language impairment 1",
          "specific language impairment QTL, 1",
          "specific language impairment quantitative trait locus on chromosome 16"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0011710"
    },
    {
      "id": 12798,
      "label": "specific language impairment 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3105
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0011711"
    },
    {
      "id": 12864,
      "label": "specific language impairment 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3105
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:375953",
          "OMIM:607134",
          "UMLS:C1846719"
        ],
        "synonyms": [
          "SLI3",
          "specific language impairment 3",
          "specific language impairment QTL, 3",
          "specific language impairment quantitative trait locus on chromosome 13"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0011780"
    },
    {
      "id": 13957,
      "label": "specific language impairment 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3105
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:393910",
          "MESH:C567288",
          "OMIM:612514",
          "UMLS:C2675874"
        ],
        "synonyms": [
          "SLI4",
          "specific language impairment 4"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012917"
    },
    {
      "id": 15191,
      "label": "specific language impairment 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3105
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0005425",
          "MEDGEN:815813",
          "OMIM:615432",
          "UMLS:C3809483"
        ],
        "synonyms": [
          "SLI5",
          "specific language impairment 5",
          "specific language impairment type 5"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A communication disorder that involves the processing of linguistic information."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014184"
    }
  ],
  "roots": [
    {
      "id": 6521,
      "label": "language disorder"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}