{
  "id": 20125,
  "label": "congenital short bowel syndrome, autosomal recessive",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020718",
  "properties": {
    "xrefs": [
      "GARD:0018585",
      "OMIM:615237"
    ],
    "synonyms": [
      "CSBS",
      "congenital short bowel syndrome",
      "congenital short bowel syndrome 1",
      "congenital short bowel syndrome due to CLMP variation"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ]
  },
  "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": 15106,
      "label": "congenital short bowel syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20383,
        21546
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016592",
          "MEDGEN:1784105",
          "Orphanet:2301",
          "SCTID:715201005",
          "UMLS:C5441717",
          "icd11.foundation:1672462112"
        ],
        "synonyms": [
          "CSBS",
          "congenital short bowel syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "Congenital short bowel syndrome is a rare intestinal disorder of neonates of unknown etiology. Patients are born with a short small bowel (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhea, vomiting and failure to thrive."
      },
      "child_count": 4,
      "reference_id": "MONDO:0014097"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 15106,
      "label": "congenital short bowel syndrome"
    }
  ]
}