{
  "id": 9013,
  "label": "gastric mucosal hypertrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007652",
  "properties": {
    "xrefs": [
      "DOID:8757",
      "EFO:1000946",
      "GARD:0002436",
      "ICD9:535.2",
      "ICD9:535.20",
      "ICD9:535.21",
      "MEDGEN:4844",
      "MESH:D005758",
      "MedDRA:10017807",
      "MedDRA:10017868",
      "NCIT:C67277",
      "NORD:1432",
      "OMIM:137280",
      "Orphanet:2494",
      "SCTID:60002000",
      "UMLS:C0017155",
      "icd11.foundation:1343994188"
    ],
    "synonyms": [
      "MENETRIER disease",
      "Menetrier Disease",
      "Menetrier disease",
      "Menetrier's disease",
      "Ménétrier disease",
      "giant hypertrophic gastritis",
      "hypertrophic gastritis",
      "hypertrophic gastropathy",
      "hypoproteinemic hypertrophic gastropathy",
      "gastritis, familial giant hypertrophic",
      "gastroenteropathy, protein losing",
      "giant hypertrophic gastropathy",
      "giant hypertrophy of the gastric mucosa"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "A rare premalignant hyperproliferative gastropathy characterized by massive overgrowth of foveolar cells in the gastric lining, resulting in large gastric folds, and manifesting with epigastric pain, nausea, vomiting, peripheral edema and, less commonly, anorexia and weight loss."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "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": 6709,
      "label": "gastritis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6115,
        20399
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4029",
          "EFO:0000217",
          "HP:0005263",
          "ICD9:535.0",
          "ICD9:535.00",
          "ICD9:535.01",
          "ICD9:535.4",
          "ICD9:535.40",
          "ICD9:535.41",
          "MEDGEN:4843",
          "MESH:D005756",
          "NCIT:C26780",
          "SCTID:4556007",
          "UMLS:C0017152",
          "icd11.foundation:1871672644"
        ],
        "synonyms": [
          "gastritis",
          "gastritis (disease)",
          "inflammation of stomach",
          "stomach inflammation",
          "acute gastric mucosal erosion",
          "erosive gastritis",
          "erosive gastropathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "Inflammation of the stomach."
      },
      "child_count": 32,
      "reference_id": "MONDO:0004966"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 6709,
      "label": "gastritis"
    }
  ]
}