{
  "id": 19926,
  "label": "mosaic monosomy X",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020467",
  "properties": {
    "xrefs": [
      "GARD:0019677",
      "MEDGEN:873772",
      "Orphanet:99228",
      "SCTID:710010005",
      "UMLS:C4040907"
    ],
    "synonyms": [
      "Mosaic Turner syndrome",
      "Mosaic monosomy type X",
      "XX/XO"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19925,
      "label": "monosomy X",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19317,
        20054,
        24425
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019676",
          "MEDGEN:116607",
          "NCIT:C36630",
          "Orphanet:99226",
          "SCTID:710008008",
          "UMLS:C0242526",
          "icd11.foundation:95979116"
        ],
        "synonyms": [
          "monosomy type X"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0020466"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19925,
      "label": "monosomy X"
    }
  ]
}