{
  "id": 23325,
  "label": "intellectual developmental disorder with neuropsychiatric features",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0044322",
  "properties": {
    "xrefs": [
      "MEDGEN:1379216",
      "OMIM:617532",
      "UMLS:C4479636"
    ],
    "synonyms": [
      "intellectual developmental disorder with neuropsychiatric features",
      "IDDNPF"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Intellectual developmental disorder with neuropsychiatric features is an autosomal recessive disorder characterized by moderate intellectual disability, relatively mild seizures, and neuropsychiatric abnormalities, such as anxiety, obsessive-compulsive behavior, and autistic features. Mild facial dysmorphic features may also be present (summary by {2:Srour et al., 2017})."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24320,
      "label": "autosomal recessive syndromic intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2961,
        24319
      ],
      "type_id": 0,
      "properties": {
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal recessive form of syndromic intellectual disability."
      },
      "child_count": 14,
      "reference_id": "MONDO:0100598"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24320,
      "label": "autosomal recessive syndromic intellectual disability"
    }
  ]
}