{
  "id": 9844,
  "label": "Paris-Trousseau thrombocytopenia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008557",
  "properties": {
    "xrefs": [
      "GARD:0004224",
      "MEDGEN:365037",
      "OMIM:188025",
      "Orphanet:851",
      "UMLS:C1956093",
      "icd11.foundation:1441183910"
    ],
    "synonyms": [
      "thrombocytopenia, Paris-Trousseau type, Isolated cases",
      "Paris-Trousseau syndrome",
      "TCPT",
      "chromosome 11q23 deletion syndrome",
      "thrombocytopenia Paris-Trousseau type",
      "thrombocytopenia, Paris-TROUSSEAU type"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Paris-Trousseau thrombocytopenia (TCPT) is a contiguous gene syndrome characterized by mild bleeding tendency, variable thrombocytopenia (THC), dysmorphic facies, abnormal giant alpha-granules in platelets and dysmegakaryopoiesis."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17329,
      "label": "partial deletion of the long arm of chromosome 11",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17301
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GTR:AN0100478",
          "GTR:AN0100479",
          "GTR:AN0100480",
          "MEDGEN:419905",
          "MESH:C538296",
          "NCIT:C37312",
          "Orphanet:262092",
          "UMLS:C2931804",
          "icd11.foundation:237602200"
        ],
        "synonyms": [
          "partial deletion of chromosome 11q",
          "partial deletion of the long arm of chromosome type 11",
          "partial monosomy of chromosome 11q",
          "partial monosomy of the long arm of chromosome 11",
          "11q deletion",
          "11q monosomy",
          "Deletion 11q partial",
          "chromosome 11q deletion",
          "chromosome 11q partial deletion",
          "del(11q)",
          "deletion 11q",
          "loss of chromosome 11q",
          "monosomy 11q",
          "monosomy 11q partial",
          "partial monosomy 11q"
        ],
        "definition": "A cytogenetic abnormality that refers to the allelic loss of all or part of the long arm of chromosome 11."
      },
      "child_count": 5,
      "reference_id": "MONDO:0016910"
    },
    {
      "id": 19741,
      "label": "alpha granule disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23981
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019469",
          "MEDGEN:1842309",
          "Orphanet:98455",
          "UMLS:C5681720",
          "icd11.foundation:237567451"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0020117"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17329,
      "label": "partial deletion of the long arm of chromosome 11"
    },
    {
      "id": 19741,
      "label": "alpha granule disease"
    }
  ]
}