{
  "id": 12306,
  "label": "childhood apraxia of speech",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011184",
  "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"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16807,
      "label": "specific language disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16806
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1631585",
          "MESH:D000080888",
          "Orphanet:211053",
          "UMLS:C4553954"
        ],
        "synonyms": [
          "dysphasia",
          "specific language disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0016226"
    },
    {
      "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": 16807,
      "label": "specific language disorder"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}