{
  "id": 16807,
  "label": "specific language disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016226",
  "properties": {
    "xrefs": [
      "MEDGEN:1631585",
      "MESH:D000080888",
      "Orphanet:211053",
      "UMLS:C4553954"
    ],
    "synonyms": [
      "dysphasia",
      "specific language disorder"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 16806,
      "label": "specific learning disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:871302",
          "MESH:D000067559",
          "Orphanet:211047",
          "UMLS:C4025790"
        ],
        "synonyms": [
          "specific learning difficulty",
          "specific learning disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Diagnosed when there are specific deficits in an individualbs ability to perceive or process information efficiently and accurately. This disorder first manifests during the years of formal schooling and is characterized by persistent and impairing difficulties with learning foundational academic skills in reading, writing, and/or math. The individualbs performance of the affected academic skills is well below average for age, or acceptable performance levels are achieved only with extraordinary effort. Specific learning disorder may occur in individuals identified as intellectually gifted and manifest only when the learning demands or assessment procedures (e.g., timed tests) pose barriers that cannot be overcome by their innate intelligence and compensatory strategies. For all individuals, specific learning disorder can produce lifelong impairments in activities dependent on the skills, including occupational performance. (from dsm-V)"
      },
      "child_count": 2,
      "reference_id": "MONDO:0016225"
    }
  ],
  "children": [
    {
      "id": 11957,
      "label": "familial developmental dysphasia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4370,
        16807
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0001823",
          "MEDGEN:374015",
          "MESH:C563997",
          "OMIM:600117",
          "Orphanet:1799",
          "SCTID:721220004",
          "UMLS:C1838630"
        ],
        "synonyms": [
          "Billard-Toutain-Maheut syndrome",
          "FOXP2-associated dysphasia",
          "developmental dysphasia familial",
          "developmental language disorder",
          "dysphasia, familial developmental",
          "specific language impairment"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Familial developmental dysphasia is a severe form of developmental verbal apraxia characterized by a deficit in spontaneous speech, writing, grammatical judgment and repetition, defective articulation, moderate to severe degree of dyspraxia, a reduced use of consonant clusters, and comprehension delay. Hearing and intelligence are normal."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010821"
    },
    {
      "id": 12306,
      "label": "childhood apraxia of speech",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16807,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111275",
          "GARD:0012889",
          "ICD9:315.39",
          "MEDGEN:152917",
          "OMIM:602081",
          "Orphanet:209908",
          "SCTID:229703009",
          "UMLS:C0750927",
          "icd11.foundation:1590154825"
        ],
        "synonyms": [
          "CAS",
          "childhood apraxia of speech",
          "developmental verbal dyspraxia",
          "speech and language disorder with orofacial dyspraxia",
          "speech-language disorder type 1",
          "SPCH1",
          "articulatory apraxia",
          "das",
          "developmental apraxia of speech",
          "developmental verbal apraxia",
          "speech-language disorder 1",
          "speech-language disorder-1"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0011184"
    }
  ],
  "roots": [
    {
      "id": 16806,
      "label": "specific learning disability"
    }
  ]
}