{
  "id": 10370,
  "label": "duodenal atresia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009126",
  "properties": {
    "xrefs": [
      "DOID:0080216",
      "GARD:0000054",
      "HP:0002247",
      "ICD9:751.1",
      "MEDGEN:75602",
      "MESH:C535720",
      "MedDRA:10013812",
      "NCIT:C101025",
      "NORD:1066",
      "OMIM:223400",
      "Orphanet:1203",
      "SCTID:51118003",
      "UMLS:C0266174",
      "icd11.foundation:295550633"
    ],
    "synonyms": [
      "Duodenal Atresia or Stenosis",
      "atresia of duodenum",
      "congenital atresia of duodenum",
      "congenital duodenal atresia",
      "duodenal atresia",
      "duodenal atresia (disease)",
      "duodenal stenosis"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "Duodenal atresia is an embryopathy of the cranial intestine that leads to a complete absence of the duodenal lumen."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3302,
      "label": "intestinal atresia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6756
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10486",
          "HP:0011100",
          "MEDGEN:7129",
          "MESH:D007409",
          "NCIT:C84790",
          "UMLS:C0021828"
        ],
        "synonyms": [
          "atresia of the intestine",
          "congenital intestinal atresia",
          "intestinal atresia",
          "intestinal atresia (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A congenital malformation characterized by the absence of a normal opening in a part of the intestine. It can occur either in the small or the large intestine."
      },
      "child_count": 2,
      "reference_id": "MONDO:0001045"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29380
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD10CM:Q00-Q99",
          "MEDGEN:1843482",
          "UMLS:C0694457"
        ],
        "definition": "Any disease or disorder that disrupts the process development of an anatomical structure. Can be due to genetic or environmental causes. Typically happens during embryogenesis, but also includes post-embryonic development."
      },
      "child_count": 190,
      "reference_id": "MONDO:0021147"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3302,
      "label": "intestinal atresia"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis"
    }
  ]
}