{
  "id": 14388,
  "label": "congenital dyserythropoietic anemia type 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013355",
  "properties": {
    "xrefs": [
      "DOID:0111400",
      "GARD:0017344",
      "MEDGEN:462276",
      "OMIM:613673",
      "Orphanet:293825",
      "SCTID:719453009",
      "UMLS:C3150926"
    ],
    "synonyms": [
      "CDA IV",
      "CDA due to KLF1 mutation",
      "CDA type 4",
      "CDA type IV",
      "CDAN4",
      "congenital dyserythropoietic anemia due to KLF1 mutation",
      "congenital dyserythropoietic anemia type 4",
      "dyserythropoietic anemia, congenital, type IV",
      "CDA, type 4",
      "anemia, congenital dyserythropoietic, type 4",
      "anemia, congenital dyserythropoietic, type IV"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Congenital dyserythropoietic anemia type IV (CDA IV) is a newly discovered form of CDA characterized by ineffective erythropoiesis and hemolysis that leads to severe anemia at birth."
  },
  "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"
    }
  ]
}