{
  "id": 25465,
  "label": "intellectual developmental disorder, autosomal dominant 70",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0859333",
  "properties": {
    "xrefs": [
      "DOID:0061043",
      "MEDGEN:1824044",
      "OMIM:620157",
      "UMLS:C5774271"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23914,
      "label": "intellectual disability, autosomal dominant",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        3324,
        24226
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "OMIMPS:156200"
        ],
        "synonyms": [
          "mental retardation, autosomal dominant",
          "autosomal dominant intellectual disability"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 87,
      "reference_id": "MONDO:0100172"
    },
    {
      "id": 25061,
      "label": "SETD2-related neurodevelopmental disorder without or with macrocephaly/overgrowth",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3324,
        24226
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "SETD2-related neurodevelopmental disorder without or with macrocephaly/overgrowth"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neurodevelopmental disorder caused by heterozygous variants in SETD2 and characterized by intellectual disability or developmental delay, motor delay, speech delay, hypotonia, autism spectrum disorder, attention deficit disorder, and sometimes features such as macrocephaly, overgrowth, and dysmorphic features."
      },
      "child_count": 4,
      "reference_id": "MONDO:0800477"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23914,
      "label": "intellectual disability, autosomal dominant"
    },
    {
      "id": 25061,
      "label": "SETD2-related neurodevelopmental disorder without or with macrocephaly/overgrowth"
    }
  ]
}