{
  "id": 19219,
  "label": "pelvis syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019388",
  "properties": {
    "xrefs": [
      "GARD:0019045",
      "MEDGEN:1374037",
      "Orphanet:83628",
      "SCTID:725138002",
      "UMLS:C4510867",
      "icd11.foundation:1311821224"
    ],
    "synonyms": [
      "LUMBAR syndrome",
      "Lower body hemangioma-urogenital anomalies-myelopathy-bony deformities-anorectal and arterial malformations-renal anomalies syndrome",
      "SACRAL syndrome",
      "perineal hemangioma-external genitalia malformations-lipomyelomeningocele-vesicorenal abnormalities-imperforate anus syndrome",
      "urorectal septum malformation sequence"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "PELVIS is an acronym defining the association of Perineal hemangioma, External genitalia malformations, Lipomyelomeningocele, Vesicorenal abnormalities, Imperforate anus, and Skin tag. Eleven cases have been reported."
  },
  "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": 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": 21330,
      "label": "vascular neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21585
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:129202",
          "NCIT:C7388",
          "UMLS:C0282607"
        ],
        "synonyms": [
          "neoplasm of vascular system",
          "neoplasm of vascular tissue",
          "neoplasms, vascular",
          "tumor of vascular system",
          "tumor of vascular tissue",
          "tumors, vascular",
          "tumour of vascular system",
          "tumour of vascular tissue",
          "vascular neoplasm",
          "vascular neoplasms",
          "vascular system neoplasm",
          "vascular system neoplasm (disease)",
          "vascular system tumor",
          "vascular system tumour",
          "vascular tissue neoplasm",
          "vascular tissue tumor",
          "vascular tissue tumour",
          "vascular tumor",
          "vascular tumors",
          "vascular tumour",
          "vascular tumours"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A benign, intermediate, or malignant neoplasm arising from vascular tissue including arteries, veins, venous sinuses, lymphatic vessels, arterioles and capillaries. It may occur in essentially any body location and is characterized by the presence of vascular channel formation and endothelial cells."
      },
      "child_count": 16,
      "reference_id": "MONDO:0024296"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 16089,
      "label": "multiple congenital anomalies/dysmorphic syndrome without intellectual disability"
    },
    {
      "id": 21330,
      "label": "vascular neoplasm"
    }
  ]
}