{
  "id": 6965,
  "label": "inflammatory bowel disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0005265",
  "properties": {
    "xrefs": [
      "DOID:0050589",
      "EFO:0003767",
      "ICD9:558.9",
      "MEDGEN:43877",
      "MESH:D015212",
      "NANDO:2100259",
      "NCIT:C3138",
      "OMIMPS:266600",
      "SCTID:24526004",
      "UMLS:C0021390"
    ],
    "synonyms": [
      "IBD",
      "autoimmune bowel disorder",
      "inflammatory bowel disease"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "A spectrum of small and large bowel inflammatory diseases of unknown etiology. It includes Crohn's disease, ulcerative colitis, and colitis of indeterminate type."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 40,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 6756,
      "label": "intestinal disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6151
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5295",
          "EFO:0009431",
          "ICD9:520-579",
          "ICD9:560-569",
          "ICD9:564",
          "ICD9:564.4",
          "ICD9:569",
          "ICD9:569.4",
          "ICD9:569.49",
          "ICD9:569.89",
          "ICD9:569.9",
          "ICD9:570-579",
          "ICD9:575",
          "MEDGEN:7130",
          "MESH:D007410",
          "NCIT:C26801",
          "SCTID:85919009",
          "UMLS:C0021831"
        ],
        "synonyms": [
          "disease of intestine",
          "disease or disorder of intestine",
          "disorder of intestine",
          "intestinal disease",
          "intestinal disorder",
          "intestine disease",
          "intestine disease or disorder",
          "disease, intestinal",
          "diseases, intestinal"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A non-neoplastic or neoplastic disorder that affects the small or large intestine."
      },
      "child_count": 58,
      "reference_id": "MONDO:0005020"
    },
    {
      "id": 6778,
      "label": "immune system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2914",
          "EFO:0000540",
          "ICD9:279",
          "ICD9:279.1",
          "ICD9:279.10",
          "ICD9:279.19",
          "ICD9:279.4",
          "ICD9:279.49",
          "ICD9:279.8",
          "ICD9:279.9",
          "MEDGEN:5759",
          "MESH:D007154",
          "NANDO:1100004",
          "NANDO:2100202",
          "NCIT:C3507",
          "SCTID:414029004",
          "UMLS:C0021053"
        ],
        "synonyms": [
          "disease of immune system",
          "disease or disorder of immune system",
          "disorder of immune system",
          "immune disease",
          "immune disorder",
          "immune dysfunction",
          "immune system disease or disorder",
          "immune system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A disorder resulting from an abnormality in the immune system."
      },
      "child_count": 47,
      "reference_id": "MONDO:0005046"
    }
  ],
  "children": [
    {
      "id": 6749,
      "label": "Crohn disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8778",
          "EFO:0000384",
          "ICD10CM:K50",
          "ICD9:555.1",
          "MEDGEN:3664",
          "MESH:D003424",
          "NANDO:1200444",
          "NANDO:1200446",
          "NANDO:2200921",
          "NCIT:C2965",
          "Orphanet:206",
          "SCTID:7620006",
          "UMLS:C0010346",
          "icd11.foundation:1267652425"
        ],
        "synonyms": [
          "Crohn disease",
          "Crohn's disease",
          "Crohn's disease of large bowel",
          "paediatric Crohn's disease",
          "pediatric Crohn's disease",
          "regional enteritis"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A gastrointestinal disorder characterized by chronic inflammation involving all layers of the intestinal wall, noncaseating granulomas affecting the intestinal wall and regional lymph nodes, and transmural fibrosis. Crohn disease most commonly involves the terminal ileum; the colon is the second most common site of involvement."
      },
      "child_count": 5,
      "reference_id": "MONDO:0005011"
    },
    {
      "id": 6986,
      "label": "colitis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4384,
        5340,
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060180",
          "EFO:0003872",
          "HP:0002583",
          "ICD9:558.9",
          "MEDGEN:40385",
          "MESH:D003092",
          "NCIT:C26723",
          "SCTID:64226004",
          "UMLS:C0009319",
          "icd11.foundation:1870792958"
        ],
        "synonyms": [
          "colitis",
          "colitis (disease)",
          "colon inflammation",
          "inflammation of colon"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Inflammation of the colon."
      },
      "child_count": 27,
      "reference_id": "MONDO:0005292"
    },
    {
      "id": 7191,
      "label": "proctitis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4590,
        6965,
        20399
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3127",
          "EFO:0005628",
          "ICD9:569.49",
          "MEDGEN:46113",
          "MESH:D011349",
          "NCIT:C38011",
          "SCTID:3951002",
          "UMLS:C0033246"
        ],
        "synonyms": [
          "anus inflammation",
          "inflammation of anus",
          "rectitis"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory process affecting the anus. It is usually caused by sexually transmitted infectious agents and/or inflammatory bowel disease."
      },
      "child_count": 6,
      "reference_id": "MONDO:0005538"
    },
    {
      "id": 8427,
      "label": "ulcerative proctosigmoiditis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1001223",
          "ICD9:556.3",
          "MEDGEN:540639",
          "SCTID:52506002",
          "UMLS:C0267390",
          "icd11.foundation:545503130"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Inflammation of the rectum and the distal portion of the colon."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007005"
    },
    {
      "id": 9901,
      "label": "inflammatory bowel disease 11",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110894",
          "MEDGEN:393069",
          "MESH:C567154",
          "OMIM:191390",
          "UMLS:C2674051"
        ],
        "synonyms": [
          "IBD11",
          "inflammatory bowel disease 11",
          "inflammatory bowel disease type 11"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 7q22."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008617"
    },
    {
      "id": 10302,
      "label": "cutaneous photosensitivity-lethal colitis syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0001633",
          "MEDGEN:347455",
          "MESH:C536224",
          "OMIM:219095",
          "Orphanet:2881",
          "UMLS:C1857449"
        ],
        "synonyms": [
          "cutaneous photosensitivity and colitis, lethal",
          "early cutaneous photosensitivity and severe colitis"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Cutaneous photosensitivity and lethal colitisis is a rare inflammatory bowel disease characterized by early cutaneous photosensitivity manifesting by sun-induced facial erythematous and vesicular lesions and severe recurent colitis which lead to untreatable diarrhea. There have been no further descriptions in the literature since 1991."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009051"
    },
    {
      "id": 11161,
      "label": "inflammatory bowel disease 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110892",
          "GARD:0009857",
          "ICD9:555.9",
          "OMIM:266600",
          "SCTID:34000006"
        ],
        "synonyms": [
          "Crohn disease-associated growth failure",
          "IBD1",
          "NOD2 inflammatory bowel disease",
          "inflammatory bowel disease (Crohn disease) 1",
          "inflammatory bowel disease 1",
          "inflammatory bowel disease 1, Crohn disease",
          "inflammatory bowel disease caused by mutation in NOD2",
          "inflammatory bowel disease type 1",
          "Crohn disease",
          "Crohn disease-associated growth failure, susceptibility to",
          "paediatric ulcerative colitis",
          "pediatric ulcerative colitis",
          "regional enteritis",
          "ulcerative colitis",
          "ulcerative colitis, paediatric",
          "ulcerative colitis, pediatric"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Any inflammatory bowel disease in which the cause of the disease is a mutation in the NOD2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009960"
    },
    {
      "id": 12213,
      "label": "inflammatory bowel disease 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110900",
          "MEDGEN:321934",
          "MESH:C563310",
          "OMIM:601458",
          "UMLS:C1832321"
        ],
        "synonyms": [
          "IBD2",
          "inflammatory bowel disease 2",
          "inflammatory bowel disease type 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 12p13.2-q24.1."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011087"
    },
    {
      "id": 12573,
      "label": "inflammatory bowel disease 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110891",
          "MEDGEN:346785",
          "MESH:C565764",
          "OMIM:604519",
          "UMLS:C1858303"
        ],
        "synonyms": [
          "IBD3",
          "inflammatory bowel disease 3",
          "inflammatory bowel disease type 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 6p21.3."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011471"
    },
    {
      "id": 12620,
      "label": "inflammatory bowel disease 7",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110882",
          "MEDGEN:381452",
          "MESH:C565353",
          "OMIM:605225",
          "UMLS:C1854573"
        ],
        "synonyms": [
          "IBD7",
          "inflammatory bowel disease 7",
          "inflammatory bowel disease type 7"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 1p36."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011521"
    },
    {
      "id": 12753,
      "label": "inflammatory bowel disease 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110889",
          "MEDGEN:342879",
          "MESH:C565234",
          "OMIM:606348",
          "UMLS:C1853438"
        ],
        "synonyms": [
          "IBD5",
          "inflammatory bowel disease 5",
          "inflammatory bowel disease type 5"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 5q31."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011661"
    },
    {
      "id": 12788,
      "label": "inflammatory bowel disease 8",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110904",
          "MEDGEN:335753",
          "MESH:C564682",
          "OMIM:606668",
          "UMLS:C1847719"
        ],
        "synonyms": [
          "IBD8",
          "inflammatory bowel disease 8",
          "inflammatory bowel disease type 8"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 16p."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011699"
    },
    {
      "id": 12789,
      "label": "inflammatory bowel disease 6",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110907",
          "MEDGEN:376191",
          "MESH:C564681",
          "OMIM:606674",
          "UMLS:C1847692"
        ],
        "synonyms": [
          "IBD6",
          "inflammatory bowel disease 6",
          "inflammatory bowel disease type 6"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 19p13."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011700"
    },
    {
      "id": 12790,
      "label": "inflammatory bowel disease 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110903",
          "MEDGEN:339822",
          "MESH:C564680",
          "OMIM:606675",
          "UMLS:C1847691"
        ],
        "synonyms": [
          "IBD4",
          "inflammatory bowel disease 4",
          "inflammatory bowel disease type 4"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 14q11-q12."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011701"
    },
    {
      "id": 13108,
      "label": "inflammatory bowel disease 9",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110886",
          "MEDGEN:324926",
          "MESH:C563926",
          "OMIM:608448",
          "UMLS:C1838019"
        ],
        "synonyms": [
          "IBD9",
          "inflammatory bowel disease 9",
          "inflammatory bowel disease type 9"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 3p26."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012040"
    },
    {
      "id": 13657,
      "label": "inflammatory bowel disease 10",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110885",
          "MEDGEN:370205",
          "MESH:C567021",
          "OMIM:611081",
          "UMLS:C1970207"
        ],
        "synonyms": [
          "ATG16L1 inflammatory bowel disease",
          "IBD10",
          "inflammatory bowel disease (Crohn disease) 10",
          "inflammatory bowel disease 10",
          "inflammatory bowel disease caused by mutation in ATG16L1",
          "inflammatory bowel disease type 10"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Any inflammatory bowel disease in which the cause of the disease is a mutation in the ATG16L1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012610"
    },
    {
      "id": 13869,
      "label": "inflammatory bowel disease 12",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110887",
          "MEDGEN:436861",
          "MESH:C567388",
          "OMIM:612241",
          "UMLS:C2677105"
        ],
        "synonyms": [
          "IBD12",
          "inflammatory bowel disease 12",
          "inflammatory bowel disease type 12"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 3p21.3"
      },
      "child_count": 0,
      "reference_id": "MONDO:0012829"
    },
    {
      "id": 13871,
      "label": "inflammatory bowel disease 13",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110893",
          "MEDGEN:394202",
          "MESH:C567384",
          "OMIM:612244",
          "UMLS:C2677101"
        ],
        "synonyms": [
          "ABCB1 inflammatory bowel disease",
          "IBD13",
          "inflammatory bowel disease 13",
          "inflammatory bowel disease caused by mutation in ABCB1",
          "inflammatory bowel disease type 13"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Any inflammatory bowel disease in which the cause of the disease is a mutation in the ABCB1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012831"
    },
    {
      "id": 13872,
      "label": "inflammatory bowel disease 14",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110895",
          "MEDGEN:436860",
          "MESH:C567383",
          "OMIM:612245",
          "UMLS:C2677100"
        ],
        "synonyms": [
          "IBD14",
          "IRF5 inflammatory bowel disease",
          "inflammatory bowel disease 14",
          "inflammatory bowel disease caused by mutation in IRF5",
          "inflammatory bowel disease type 14"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Any inflammatory bowel disease in which the cause of the disease is a mutation in the IRF5 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012832"
    },
    {
      "id": 13877,
      "label": "inflammatory bowel disease 15",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110897",
          "MEDGEN:383025",
          "MESH:C567381",
          "OMIM:612255",
          "UMLS:C2677094"
        ],
        "synonyms": [
          "IBD15",
          "inflammatory bowel disease 15",
          "inflammatory bowel disease type 15"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 10q21."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012837"
    },
    {
      "id": 13878,
      "label": "inflammatory bowel disease 16",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110896",
          "MEDGEN:383024",
          "MESH:C567380",
          "OMIM:612259",
          "UMLS:C2677093"
        ],
        "synonyms": [
          "IBD16",
          "inflammatory bowel disease 16",
          "inflammatory bowel disease type 16"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 9q32."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012838"
    },
    {
      "id": 13880,
      "label": "inflammatory bowel disease 17",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110883",
          "MEDGEN:436857",
          "MESH:C567378",
          "OMIM:612261",
          "UMLS:C2677091"
        ],
        "synonyms": [
          "IBD17",
          "IL23R inflammatory bowel disease",
          "inflammatory bowel disease 17",
          "inflammatory bowel disease 17, protection against",
          "inflammatory bowel disease caused by mutation in IL23R",
          "inflammatory bowel disease type 17"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Any inflammatory bowel disease in which the cause of the disease is a mutation in the IL23R gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012840"
    },
    {
      "id": 13881,
      "label": "inflammatory bowel disease 18",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110888",
          "MEDGEN:393655",
          "MESH:C567377",
          "OMIM:612262",
          "UMLS:C2677090"
        ],
        "synonyms": [
          "IBD18",
          "inflammatory bowel disease 18",
          "inflammatory bowel disease type 18"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 5p13.1."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012841"
    },
    {
      "id": 13885,
      "label": "inflammatory bowel disease 19",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110890",
          "MEDGEN:393652",
          "MESH:C567372",
          "OMIM:612278",
          "UMLS:C2677079"
        ],
        "synonyms": [
          "IBD19",
          "IRGM inflammatory bowel disease",
          "inflammatory bowel disease (Crohn disease) 19",
          "inflammatory bowel disease 19",
          "inflammatory bowel disease caused by mutation in IRGM",
          "inflammatory bowel disease type 19"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Any inflammatory bowel disease in which the cause of the disease is a mutation in the IRGM gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012845"
    },
    {
      "id": 13892,
      "label": "inflammatory bowel disease 20",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110898",
          "MEDGEN:394126",
          "MESH:C567361",
          "OMIM:612288",
          "UMLS:C2676781"
        ],
        "synonyms": [
          "IBD20",
          "inflammatory bowel disease 20",
          "inflammatory bowel disease type 20"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 10q23-q24."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012852"
    },
    {
      "id": 13915,
      "label": "inflammatory bowel disease 21",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110906",
          "MEDGEN:436705",
          "MESH:C567338",
          "OMIM:612354",
          "UMLS:C2676507"
        ],
        "synonyms": [
          "IBD21",
          "inflammatory bowel disease 21",
          "inflammatory bowel disease type 21"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 18p11."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012875"
    },
    {
      "id": 13926,
      "label": "inflammatory bowel disease 22",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110905",
          "MEDGEN:382862",
          "MESH:C567327",
          "OMIM:612380",
          "UMLS:C2676485"
        ],
        "synonyms": [
          "IBD22",
          "inflammatory bowel disease 22",
          "inflammatory bowel disease type 22"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 17q21.2."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012886"
    },
    {
      "id": 13927,
      "label": "inflammatory bowel disease 23",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110884",
          "MEDGEN:382861",
          "MESH:C567326",
          "OMIM:612381",
          "UMLS:C2676484"
        ],
        "synonyms": [
          "IBD23",
          "inflammatory bowel disease 23",
          "inflammatory bowel disease type 23"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 1q32.1."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012887"
    },
    {
      "id": 13980,
      "label": "inflammatory bowel disease 24",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110908",
          "MEDGEN:393404",
          "MESH:C567252",
          "OMIM:612566",
          "UMLS:C2675509"
        ],
        "synonyms": [
          "IBD24",
          "inflammatory bowel disease 24",
          "inflammatory bowel disease type 24"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome 20q13."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012940"
    },
    {
      "id": 14013,
      "label": "inflammatory bowel disease 26",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110901",
          "MEDGEN:382561",
          "MESH:C567217",
          "OMIM:612639",
          "UMLS:C2675249"
        ],
        "synonyms": [
          "IBD26",
          "inflammatory bowel disease 26",
          "inflammatory bowel disease type 26"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 12q15."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012973"
    },
    {
      "id": 14051,
      "label": "inflammatory bowel disease 27",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110902",
          "MEDGEN:412579",
          "MESH:C567559",
          "OMIM:612796",
          "UMLS:C2748550"
        ],
        "synonyms": [
          "IBD27",
          "inflammatory bowel disease 27",
          "inflammatory bowel disease type 27"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease that has material basis in variation in the chromosome region 13q13.3"
      },
      "child_count": 0,
      "reference_id": "MONDO:0013012"
    },
    {
      "id": 16100,
      "label": "undetermined colitis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019840",
          "MEDGEN:1842621",
          "Orphanet:103920",
          "UMLS:C5681748"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Underterminate colitis designates a rare inflammatory bowel disease that clinically resembles CrohnBs disease and ulcerative colitis but that cannot be diagnosed as one of them after examination of an intestinal resection specimen."
      },
      "child_count": 0,
      "reference_id": "MONDO:0015176"
    },
    {
      "id": 16373,
      "label": "cap polyposis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020038",
          "MEDGEN:929640",
          "Orphanet:160148",
          "SCTID:720604008",
          "UMLS:C4303971",
          "icd11.foundation:1387262691"
        ],
        "synonyms": [
          "Cap inflammatory polyposis",
          "eroded polypoid hyperplasia",
          "inflammatory myoglandular polyps",
          "polypoid prolapsing folds"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Cap polyposis (CP) is a rare colorectal disease characterized by multiple inflammatory polyps that predominantly affect the rectosigmoid area and that manifests primarily as rectal bleeding with abnormal transit, constipation and diarrhea."
      },
      "child_count": 0,
      "reference_id": "MONDO:0015565"
    },
    {
      "id": 17037,
      "label": "IL10-related early-onset inflammatory bowel disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5658,
        6965,
        7203,
        21247
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0013016",
          "MEDGEN:1661450",
          "NANDO:2200446",
          "Orphanet:238569",
          "UMLS:C4749850"
        ],
        "synonyms": [
          "IL10-related early-onset IBD",
          "IL10-related early-onset inflammatory bowel disease",
          "immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome",
          "autosomal recessive early-onset IBD",
          "autosomal recessive early-onset inflammatory bowel disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A rare immune dysregulation disease with immunodeficiency characterized by severe, progressive infantile onset inflammatory bowel disease with pancolitis, perianal disease (ulceration, fistulae), recurrent respiratory, genitourinary and cutaneous infections, arthritis and a high risk of B-cell lymphoma."
      },
      "child_count": 8,
      "reference_id": "MONDO:0016542"
    },
    {
      "id": 17718,
      "label": "neonatal inflammatory skin and bowel disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6965,
        19129,
        19503,
        21247,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017355",
          "MEDGEN:1648296",
          "OMIMPS:614328",
          "Orphanet:294023",
          "UMLS:C4751120"
        ],
        "synonyms": [
          "inflammatory skin and bowel disease, neonatal"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Neonatal inflammatory skin and bowel disease is a rare, life-threatening, autoinflammatory syndrome with immune deficiency disorder characterized by early-onset, life-long inflammation, affecting the skin and bowel, associated with recurrent infections. Patients present perioral and perianal psoriasiform erythema and papular eruption with pustules, failure to thrive associated with chronic malabsorptive diarrhea, intercurrent gastrointestinal infections and feeding troubles, as well as absent, short or broken hair and trichomegaly. Recurrent cutaneous and pulmonary infections lead to recurrent blepharitis, otitis externa and bronchiolitis."
      },
      "child_count": 10,
      "reference_id": "MONDO:0017411"
    },
    {
      "id": 21879,
      "label": "inflammatory bowel disease (infantile ulcerative colitis) 31, autosomal recessive",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1783277",
          "OMIM:619398",
          "UMLS:C5444224"
        ],
        "synonyms": [
          "IBD31",
          "inflammatory bowel disease (infantile ulcerative colitis) 31",
          "inflammatory bowel disease (infantile ulcerative colitis) 31, autosomal recessive",
          "inflammatory bowel disease, early-onset, autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030314"
    },
    {
      "id": 22714,
      "label": "inflammatory bowel disease 30",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112154",
          "MEDGEN:1737985",
          "OMIM:619079",
          "UMLS:C5436750"
        ],
        "synonyms": [
          "IBD30",
          "inflammatory bowel disease (Crohn disease) 30"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "An inflammatory bowel disease characterized by abdominal pain and watery or bloody diarrhea, with changes in the intestinal tract consistent with Crohn disease that has material basis in heterozygous mutation in the CARD8 gene on chromosome 19q13.33."
      },
      "child_count": 0,
      "reference_id": "MONDO:0033643"
    },
    {
      "id": 22829,
      "label": "TRIM22-related inflammatory bowel disease",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022395",
          "MEDGEN:1842464",
          "Orphanet:597201",
          "UMLS:C5680271"
        ],
        "synonyms": [
          "TRIM22-related IBD"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Any inflammatory bowel disease in which the cause of the disease is a mutation in the TRIM22 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0035362"
    },
    {
      "id": 22830,
      "label": "ALPI-related inflammatory bowel disease",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022400",
          "MEDGEN:1842198",
          "Orphanet:597887",
          "UMLS:C5681586"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Any inflammatory bowel disease in which the cause of the disease is a mutation in the ALPI gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0035370"
    },
    {
      "id": 23647,
      "label": "inflammatory bowel disease 29",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6965
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112155",
          "MEDGEN:1648318",
          "OMIM:618077",
          "UMLS:C4748083"
        ],
        "synonyms": [
          "inflammatory bowel disease 29",
          "IBD29"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054849"
    }
  ],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 6756,
      "label": "intestinal disorder"
    },
    {
      "id": 6778,
      "label": "immune system disorder"
    }
  ]
}