{
  "id": 17074,
  "label": "familial intestinal malrotation-facial anomalies syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016583",
  "properties": {
    "xrefs": [
      "Orphanet:2454"
    ],
    "synonyms": [
      "Stalker-Chitayat syndrome",
      "Stalker Chitayat syndrome",
      "intestinal malrotation facial anomalies familial type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 9943,
      "label": "volvulus of midgut",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6756
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027787",
          "MEDGEN:113153",
          "MESH:C562456",
          "NCIT:C98961",
          "OMIM:193250",
          "Orphanet:508410",
          "SCTID:458422009",
          "UMLS:C0221210"
        ],
        "synonyms": [
          "congenital malrotation of intestine",
          "intestinal malrotation",
          "volvulus of midgut",
          "intestinal malrotation, familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A congenital abnormality in which the intestine is abnormally rotated (twisted). It may result in intestinal obstruction."
      },
      "child_count": 2,
      "reference_id": "MONDO:0008666"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29380
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD10CM:Q00-Q99",
          "MEDGEN:1843482",
          "UMLS:C0694457"
        ],
        "definition": "Any disease or disorder that disrupts the process development of an anatomical structure. Can be due to genetic or environmental causes. Typically happens during embryogenesis, but also includes post-embryonic development."
      },
      "child_count": 190,
      "reference_id": "MONDO:0021147"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 9943,
      "label": "volvulus of midgut"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis"
    }
  ]
}