{
  "id": 10692,
  "label": "multiple intestinal atresia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009465",
  "properties": {
    "xrefs": [
      "GARD:0003013",
      "ICD9:751.8",
      "MEDGEN:65090",
      "MESH:C562441",
      "MedDRA:10028210",
      "Orphanet:2300",
      "SCTID:95472001",
      "UMLS:C0220744"
    ],
    "synonyms": [
      "isolated multiple intestinal atresia",
      "multiple intestinal atresia",
      "intestinal atresia multiple",
      "intestinal atresia, multiple",
      "multiple gastrointestinal atresias"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "A rare form of intestinal atresia characterized by the presence of numerous atresic segments in the small bowel (duodenum) or large bowel and leading to symptoms of intestinal obstruction: vomiting, abdominal bloating and inability to pass meconium in newborns."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "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": [
    {
      "id": 22059,
      "label": "gastrointestinal defect and immunodeficiency syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        10692
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027932",
          "MEDGEN:1708537",
          "OMIMPS:243150",
          "Orphanet:436252",
          "UMLS:C5234880"
        ],
        "synonyms": [
          "hereditary multiple intestinal atresia"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A rare hereditary disease characterized by intestinal obstruction and profound combined immune deficiency."
      },
      "child_count": 4,
      "reference_id": "MONDO:0030831"
    }
  ],
  "roots": [
    {
      "id": 3302,
      "label": "intestinal atresia"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis"
    }
  ]
}