{
  "id": 8522,
  "label": "congenital dyserythropoietic anemia type 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007109",
  "properties": {
    "xrefs": [
      "DOID:0111399",
      "GARD:0002002",
      "ICD9:285.8",
      "MEDGEN:1801596",
      "NANDO:1200888",
      "OMIM:105600",
      "Orphanet:98870",
      "SCTID:26409005",
      "UMLS:C5676874"
    ],
    "synonyms": [
      "CDA III",
      "CDA type 3",
      "CDA type III",
      "congenital dyserythropoietic anemia type 3",
      "dyserythropoietic anemia, congenital, type III",
      "CDA 3",
      "CDAN3",
      "Erythroreticulosis, hereditary benign",
      "anaemia with multinucleated erythroblasts",
      "anemia with multinucleated erythroblasts",
      "anemia, congenital dyserythropoietic, type III",
      "dyserythropoietic Anemia, congenital, type 3",
      "dyserythropoietic anemia, congenital type 3"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Congenital dyserythropoietic anemia type III (CDA III) is a rare form of CDA characterized by dyserythropoiesis, with big multinucleated erythroblasts in the bone marrow, and manifesting with mild to moderate anemia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3000,
      "label": "congenital anemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4394,
        10564
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022807",
          "MEDGEN:102361",
          "NCIT:C35228",
          "SCTID:63565007",
          "UMLS:C0158995"
        ],
        "synonyms": [
          "congenital anaemia (disease)",
          "congenital anemia",
          "congenital anemia (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Anemia, the cause of which is present at birth."
      },
      "child_count": 16,
      "reference_id": "MONDO:0000577"
    },
    {
      "id": 19232,
      "label": "congenital dyserythropoietic anemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5573
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1338",
          "GARD:0001999",
          "ICD10CM:D64.4",
          "ICD9:285.8",
          "MEDGEN:8064",
          "MESH:D000742",
          "NANDO:1200885",
          "NANDO:2100178",
          "NANDO:2200615",
          "NCIT:C84646",
          "OMIMPS:224120",
          "Orphanet:85",
          "SCTID:52951008",
          "UMLS:C0002876",
          "icd11.foundation:899830967"
        ],
        "synonyms": [
          "CDA",
          "anemia, congenital dyserythropoietic",
          "congenital dyshaematopoietic anaemia",
          "congenital dyshaematopoietic anemia",
          "dyserythropoietic anemia, congenital"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Congenital dyserythropoietic anemia (CDA) is a heterogenous group of hematological disorders of late erythropoiesis and red cell abnormalities that lead to anemia. Five types of CDA are defined: CDA I, CDA II, CDA III, CDA IV and thrombocytopenia with CDA."
      },
      "child_count": 9,
      "reference_id": "MONDO:0019403"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3000,
      "label": "congenital anemia"
    },
    {
      "id": 19232,
      "label": "congenital dyserythropoietic anemia"
    }
  ]
}