{
  "id": 24784,
  "label": "gastrointestinal defects and immunodeficiency syndrome 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800030",
  "properties": {
    "xrefs": [
      "DOID:14671",
      "GARD:0017731",
      "MEDGEN:1872649",
      "OMIM:243150",
      "UMLS:C5968858"
    ],
    "synonyms": [
      "intestinal atresia, multiple",
      "FIPA",
      "MINAT",
      "familial intestinal polyatresia syndrome",
      "multiple intestinal atresia and/or inflammatory bowel disease with or without immunodeficiency",
      "CID-MIA/early-onset IBD",
      "combined immunodeficiency-enteropathy spectrum"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "A rare genetic disease characterized by multiple intestinal atresia in association with combined immunodeficiency and inflammatory bowel disease. Clinical features include widespread atresia extending from the stomach to the rectum, homogenous calcifications in the abdominal cavity, hepatic cholestasis, cirrhosis, and chronic liver failure, hypoplastic thymus, and increased susceptibility to mainly bacteria and viruses. The immunological phenotype consists of profound generalized T-cell lymphopenia and milder natural killer cell and B-cell lymphopenia, as well as low serum levels of IgG, IgA, and IgM, with elevated serum IgE. The disease is mostly fatal in infancy or childhood."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 22059,
      "label": "gastrointestinal defect and immunodeficiency syndrome"
    }
  ]
}