{
  "id": 19947,
  "label": "Haddad syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020493",
  "properties": {
    "xrefs": [
      "GARD:0016909",
      "MEDGEN:347052",
      "Orphanet:99803",
      "SCTID:719972004",
      "UMLS:C1859049",
      "icd11.foundation:1685926536"
    ],
    "synonyms": [
      "Haddad syndrome",
      "congenital central alveolar hypoventilation-Hirschsprung disease syndrome",
      "ondine-Hirschsprung disease",
      "ondine-Hirschsprung syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "Haddad syndrome is a rare congenital disorder in which congenital central hypoventilation syndrome (CCHS), or Ondine syndrome, occurs concurrently with Hirschsprung disease."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20415,
      "label": "intestinal motility disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6756
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:586448",
          "UMLS:C0400865"
        ],
        "synonyms": [
          "disorder of intestinal motility"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A disease that has its basis in the disruption of intestinal motility."
      },
      "child_count": 15,
      "reference_id": "MONDO:0021189"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 20415,
      "label": "intestinal motility disease"
    }
  ]
}