{
  "id": 14857,
  "label": "intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013843",
  "properties": {
    "xrefs": [
      "GARD:0017418",
      "ICD9:777.1",
      "MEDGEN:1390359",
      "OMIM:614665",
      "Orphanet:314376",
      "SCTID:733447005",
      "UMLS:C4518781"
    ],
    "synonyms": [
      "meconium ileus",
      "GUCY2C meconium ileus",
      "meconium ileus caused by mutation in GUCY2C",
      "meconium ileus due to guanylate cyclase 2C deficiency"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "Any meconium ileus in which the cause of the disease is a mutation in the GUCY2C gene."
  },
  "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": 20415,
      "label": "intestinal motility disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6756
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:586448",
          "UMLS:C0400865"
        ],
        "synonyms": [
          "disorder of intestinal motility"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A disease that has its basis in the disruption of intestinal motility."
      },
      "child_count": 15,
      "reference_id": "MONDO:0021189"
    },
    {
      "id": 23656,
      "label": "meconium ileus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6365
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:473705",
          "MESH:D000074270",
          "NCIT:C98979",
          "SCTID:206523001",
          "UMLS:C2939175"
        ],
        "synonyms": [
          "meconium ileus"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "Small intestinal obstruction that results from the impaction of thick meconium in the distal small intestine."
      },
      "child_count": 2,
      "reference_id": "MONDO:0054868"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 20415,
      "label": "intestinal motility disease"
    },
    {
      "id": 23656,
      "label": "meconium ileus"
    }
  ]
}