{
  "id": 6854,
  "label": "celiac disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0005130",
  "properties": {
    "xrefs": [
      "DOID:10608",
      "EFO:0001060",
      "ICD10CM:K90.0",
      "ICD9:579.0",
      "MEDGEN:3291",
      "MESH:D002446",
      "NCIT:C26714",
      "OMIMPS:212750",
      "Orphanet:555",
      "SCTID:396331005",
      "UMLS:C0007570",
      "icd11.foundation:2005943638"
    ],
    "synonyms": [
      "celiac disease",
      "celiac sprue",
      "coeliac sprue",
      "gluten intolerance",
      "gluten-induced enteropathy",
      "non tropical sprue"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "An autoimmune genetic disorder with an unknown pattern of inheritance that primarily affects the digestive tract. It is caused by intolerance to dietary gluten. Consumption of gluten protein triggers an immune response which damages small intestinal villi and prevents adequate absorption of nutrients. Clinical signs include abdominal cramping, diarrhea or constipation and weight loss. If untreated, the clinical course may progress to malnutrition, anemia, osteoporosis and an increased risk of intestinal malignancies. However, the prognosis is favorable with successful avoidance of gluten in the diet."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 3004,
      "label": "autoimmune disorder of gastrointestinal tract",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6151,
        8586
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060031"
        ],
        "synonyms": [
          "alimentary part of gastrointestinal system autoimmune disease",
          "alimentary part of gastrointestinal system hypersensitivity reaction type II disease",
          "autoimmune disease of alimentary part of gastrointestinal system"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A hypersensitivity reaction type II disease that involves the alimentary part of gastrointestinal system."
      },
      "child_count": 14,
      "reference_id": "MONDO:0000588"
    },
    {
      "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": 20033,
      "label": "malabsorption syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6756
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0009554",
          "MEDGEN:44256",
          "MESH:D008286",
          "NCIT:C3214",
          "SCTID:32230006",
          "UMLS:C0024523"
        ],
        "synonyms": [
          "malabsorption",
          "malabsorption syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A syndrome resulting from the inadequate absorption of nutrients in the small intestine. Symptoms include abdominal pain, bloating, and diarrhea."
      },
      "child_count": 9,
      "reference_id": "MONDO:0020598"
    },
    {
      "id": 21546,
      "label": "small intestine disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6756
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:574283",
          "SCTID:119522002",
          "UMLS:C0341268"
        ],
        "synonyms": [
          "disease of small intestine",
          "disease or disorder of small intestine",
          "disorder of small intestine",
          "small intestine disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A disease that involves the small intestine."
      },
      "child_count": 10,
      "reference_id": "MONDO:0024635"
    }
  ],
  "children": [
    {
      "id": 24830,
      "label": "Lane Hamilton syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6854,
        9649,
        18954,
        22225
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026443"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ],
        "definition": "A rare concurrent association of idiopathic pulmonary hemosiderosis and celiac disease, and is typically seen in children under the age of 15."
      },
      "child_count": 0,
      "reference_id": "MONDO:0800124"
    }
  ],
  "roots": [
    {
      "id": 3004,
      "label": "autoimmune disorder of gastrointestinal tract"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 20033,
      "label": "malabsorption syndrome"
    },
    {
      "id": 21546,
      "label": "small intestine disorder"
    }
  ]
}