{
  "id": 17683,
  "label": "congenital varicella syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017372",
  "properties": {
    "xrefs": [
      "GARD:0000045",
      "ICD9:771.2",
      "MEDGEN:87473",
      "NCIT:C116800",
      "NORD:1003",
      "Orphanet:291",
      "SCTID:277644009",
      "UMLS:C0343560",
      "icd11.foundation:2071159826"
    ],
    "synonyms": [
      "antenatal varicella virus infection",
      "mother-to-child transmission of varicella syndrome",
      "Varicella embryopathy",
      "Varicella virus antenatal infection",
      "fetal effects of chickenpox",
      "fetal effects of varicella zoster virus",
      "fetal varicella infection",
      "fetal varicella zoster syndrome",
      "foetal effects of chickenpox",
      "foetal effects of varicella zoster virus",
      "foetal varicella infection",
      "foetal varicella zoster syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Fetal varicella syndrome (CVS) is an acquired developmental anomaly syndrome characterized by skin, neurological, ocular, limbs and growth defects secondary to maternal Varicella-Zoster Virus (VZV) infection."
  },
  "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": 6834,
      "label": "viral infectious disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7200
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:934",
          "EFO:0000763",
          "ICD9:060-066",
          "ICD9:066.9",
          "ICD9:078.89",
          "ICD9:079.99",
          "MESH:D014777",
          "NCIT:C3439",
          "SCTID:34014006"
        ],
        "synonyms": [
          "Viruses caused disease or disorder",
          "Viruses disease or disorder",
          "Viruses infection",
          "Viruses infectious disease",
          "infection, viral",
          "viral disease",
          "viral disorder",
          "viral infection",
          "infections, Viruses"
        ],
        "definition": "Any disease caused by a virus."
      },
      "child_count": 42,
      "reference_id": "MONDO:0005108"
    },
    {
      "id": 17014,
      "label": "infectious embryofetopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7200,
        19507
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1736309",
          "Orphanet:232035",
          "UMLS:C5439342"
        ]
      },
      "child_count": 20,
      "reference_id": "MONDO:0016511"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 6834,
      "label": "viral infectious disease"
    },
    {
      "id": 17014,
      "label": "infectious embryofetopathy"
    }
  ]
}