{
  "id": 10440,
  "label": "transient erythroblastopenia of childhood",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009197",
  "properties": {
    "xrefs": [
      "GARD:0007793",
      "ICD9:284.81",
      "MEDGEN:68670",
      "MESH:C536980",
      "NCIT:C131683",
      "OMIM:227050",
      "Orphanet:98871",
      "SCTID:191255003",
      "UMLS:C0238478"
    ],
    "synonyms": [
      "transient acquired pure red cell aplasia",
      "transient erythroblastopenia of childhood",
      "erythroblastopenia, transient",
      "familial transient erythroblastopenia of childhood",
      "tec"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "An acquired pure red cell aplasia that is self-limited. It is the most common cause of decreased red blood cell production in the pediatric population, and typically presents as a normocytic anemia with reticulocytopenia in an otherwise asymptomatic and normal child with no evidence of other causes for anemia, including blood loss, hemolysis, nutritional deficiency, or malignancy."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19739,
      "label": "primary acquired red cell aplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16404
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019465",
          "MedDRA:10038184",
          "Orphanet:98421"
        ],
        "synonyms": [
          "red cell aplasia",
          "primary autoimmune red cell aplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0020113"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19739,
      "label": "primary acquired red cell aplasia"
    }
  ]
}