{
  "id": 23694,
  "label": "vertebral, cardiac, renal, and limb defects syndrome 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0060554",
  "properties": {
    "xrefs": [
      "GARD:0018508",
      "MEDGEN:1621146",
      "OMIM:617660",
      "UMLS:C4540004"
    ],
    "synonyms": [
      "vertebral, cardiac, renal, and limb defects syndrome 1",
      "3-hydroxyanthranilic acidemia",
      "VCRL1",
      "congenital NAD deficiency Disorder 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20218,
      "label": "congenital vertebral-cardiac-renal anomalies syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7611,
        16089,
        24272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017961",
          "MEDGEN:1814457",
          "OMIMPS:617660",
          "Orphanet:521438",
          "UMLS:C5680183"
        ],
        "synonyms": [
          "VCRL",
          "vertebral, cardiac, renal, and limb defects syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 9,
      "reference_id": "MONDO:0020831"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 20218,
      "label": "congenital vertebral-cardiac-renal anomalies syndrome"
    }
  ]
}