{
  "id": 16119,
  "label": "pentasomy X",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015228",
  "properties": {
    "xrefs": [
      "GARD:0005678",
      "MEDGEN:423649",
      "MESH:C535319",
      "NCIT:C89802",
      "NORD:1565",
      "Orphanet:11",
      "SCTID:43248007",
      "UMLS:C2937419",
      "icd11.foundation:2087864894"
    ],
    "synonyms": [
      "49, XXXXX syndrome",
      "49,XXXXX syndrome",
      "Penta X Syndrome",
      "Pentasomy type X",
      "XXXXX syndrome",
      "penta X syndrome",
      "penta-X",
      "poly-X",
      "Pentasomy X syndrome",
      "chromosome X pentasomy",
      "chromosome XXXXX syndrome",
      "penta-X syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Pentasomy X is a sex chromosome anomaly caused by the presence of three extra X chromosomes in females (49,XXXXX instead of 46,XX)."
  },
  "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": 24425,
      "label": "chromosome X disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19717
      ],
      "type_id": 0,
      "properties": {
        "definition": "Chromosomal disorder in which chromosome X is affected."
      },
      "child_count": 13,
      "reference_id": "MONDO:0700027"
    },
    {
      "id": 24481,
      "label": "pentasomy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24460
      ],
      "type_id": 0,
      "properties": {
        "definition": "A chromosomal disorder consisting of the presence of three chromosomes of the same type in addition to the normal diploid number."
      },
      "child_count": 3,
      "reference_id": "MONDO:0700085"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 24425,
      "label": "chromosome X disorder"
    },
    {
      "id": 24481,
      "label": "pentasomy"
    }
  ]
}