{
  "id": 20218,
  "label": "congenital vertebral-cardiac-renal anomalies syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020831",
  "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"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 7611,
      "label": "autosomal recessive disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050737",
          "EFO:1000017",
          "ICD9:758.5",
          "MEDGEN:539209",
          "SCTID:85995004",
          "UMLS:C0265388"
        ],
        "synonyms": [
          "autosomal recessive disease or disorder",
          "autosomal recessive hereditary disease",
          "autosomal recessive hereditary disorder",
          "autosomal recessive inherited disease",
          "autosomal recessive inherited disorder",
          "disease or disorder, autosomal recessive",
          "disease, autosomal recessive",
          "recessive hereditary disorder (autosomal)"
        ],
        "definition": "Autosomal recessive form of disease."
      },
      "child_count": 219,
      "reference_id": "MONDO:0006025"
    },
    {
      "id": 16089,
      "label": "multiple congenital anomalies/dysmorphic syndrome without intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18951
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019833",
          "MEDGEN:1842829",
          "Orphanet:102285",
          "UMLS:C5680373"
        ],
        "synonyms": [
          "MCA without intellectual disability",
          "multiple congenital anomalies without intellectual disability with or without dysmorphism"
        ]
      },
      "child_count": 168,
      "reference_id": "MONDO:0015161"
    },
    {
      "id": 24272,
      "label": "cardiogenetic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6967
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "hereditary heart disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the cardiovascular system."
      },
      "child_count": 146,
      "reference_id": "MONDO:0100547"
    }
  ],
  "children": [
    {
      "id": 21850,
      "label": "vertebral, cardiac, renal, and limb defects syndrome 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20218
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018510",
          "MEDGEN:1709064",
          "OMIM:618845",
          "UMLS:C5394250"
        ],
        "synonyms": [
          "Congenital Nad Deficiency Disorder 3",
          "VCRL3",
          "VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 3",
          "vertebral, cardiac, renal, and limb defects syndrome 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030077"
    },
    {
      "id": 23694,
      "label": "vertebral, cardiac, renal, and limb defects syndrome 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20218
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0060554"
    },
    {
      "id": 23695,
      "label": "vertebral, cardiac, renal, and limb defects syndrome 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20218
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018509",
          "MEDGEN:1624065",
          "OMIM:617661",
          "UMLS:C4540014"
        ],
        "synonyms": [
          "vertebral, cardiac, renal, and limb defects syndrome 2",
          "VCRL2",
          "congenital NAD deficiency disorder 2",
          "kynureninase deficiency, complete"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0060555"
    }
  ],
  "roots": [
    {
      "id": 7611,
      "label": "autosomal recessive disease"
    },
    {
      "id": 16089,
      "label": "multiple congenital anomalies/dysmorphic syndrome without intellectual disability"
    },
    {
      "id": 24272,
      "label": "cardiogenetic disease"
    }
  ]
}