{
  "id": 18073,
  "label": "acute erythroid leukemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017858",
  "properties": {
    "xrefs": [
      "DOID:0080780",
      "EFO:0000218",
      "GARD:0009620",
      "ICD10CM:C94.0",
      "ICD9:205.80",
      "ICD9:207.00",
      "ICDO:9840/3",
      "MEDGEN:7316",
      "MESH:D004915",
      "NANDO:2200010",
      "NCIT:C8923",
      "Orphanet:318",
      "SCTID:93451002",
      "UMLS:C0023440",
      "icd11.foundation:538743484",
      "icd11.foundation:631263622"
    ],
    "synonyms": [
      "AEL",
      "AML M6",
      "FAB M6",
      "M6 acute myeloid leukaemia",
      "M6 acute myeloid leukemia",
      "acute erythroblastic leukaemia",
      "acute erythroblastic leukemia",
      "acute erythroid leukemia",
      "acute myeloid leukaemia M6",
      "acute myeloid leukemia M6",
      "erythroblastic leukaemia",
      "erythroblastic leukemia",
      "leukemia, erythroid, malignant",
      "AML-M6",
      "Di Guglielmo syndrome",
      "Di Guglielmo's syndrome",
      "Erythroleukemia",
      "acute erythroleukemia",
      "acute erythroleukemia M6a subtype",
      "acute erythroleukemia M6b subtype",
      "acute myeloid leukaemia FAB-M6",
      "acute myeloid leukemia FAB-M6"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "An acute myeloid leukemia characterized by a predominant immature erythroid population. There are two subtypes recognized: erythroleukemia and pure erythroid leukemia. (WHO, 2001)"
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 16444,
      "label": "acute myeloid leukemia by FAB classification",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18806
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012760",
          "MEDGEN:1842303",
          "NCIT:C27753",
          "Orphanet:167714",
          "UMLS:C5679583"
        ],
        "synonyms": [
          "acute myeloid leukaemia",
          "acute myeloid leukemia",
          "AML, NOS",
          "acute myeloid leukaemia NOS",
          "acute myeloid leukaemia not otherwise categorised",
          "acute myeloid leukaemia not otherwise specified",
          "acute myeloid leukemia NOS",
          "acute myeloid leukemia not otherwise categorized",
          "acute myeloid leukemia not otherwise specified",
          "acute myeloid leukemia, NOS",
          "unclassified AML",
          "unclassified acute myeloid leukaemia",
          "unclassified acute myeloid leukemia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Acute myeloid leukemias that do not fulfill the criteria for inclusion in the group of acute myeloid leukemias which have recurrent genetic abnormalities or myelodysplastic changes, or are therapy-related. This category includes entities classified according to the French-American-British classification scheme."
      },
      "child_count": 9,
      "reference_id": "MONDO:0015667"
    },
    {
      "id": 20110,
      "label": "erythroid neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19727
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025216",
          "MEDGEN:272584",
          "NCIT:C7064",
          "UMLS:C1333438"
        ],
        "synonyms": [
          "erythroid neoplasm",
          "erythroid tumor",
          "erythroid tumour"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0020703"
    }
  ],
  "children": [
    {
      "id": 25551,
      "label": "erythroleukemia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18073
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080916",
          "GARD:0026756",
          "MEDGEN:1614281",
          "NCIT:C7152",
          "UMLS:C4520840"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "An acute erythroid leukemia characterized by the presence of at least 50% erythroid precursors and at least 20% myeloblasts in the bone marrow."
      },
      "child_count": 0,
      "reference_id": "MONDO:0859598"
    }
  ],
  "roots": [
    {
      "id": 16444,
      "label": "acute myeloid leukemia by FAB classification"
    },
    {
      "id": 20110,
      "label": "erythroid neoplasm"
    }
  ]
}