{
  "id": 22874,
  "label": "mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0035639",
  "properties": {
    "xrefs": [
      "GARD:0022354",
      "ICD10CM:C92.7",
      "MEDGEN:414807",
      "Orphanet:589534",
      "UMLS:C2826037"
    ],
    "synonyms": [
      "MPAL with t(9;22)(q34.1;q11.2); BCR-ABL1"
    ],
    "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"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18103,
      "label": "inherited acute myeloid leukemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18806,
        21247
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017450",
          "MEDGEN:1634915",
          "NCIT:C7175",
          "Orphanet:319465",
          "SCTID:764940002",
          "UMLS:C4707228"
        ],
        "synonyms": [
          "Pure familial AML",
          "Pure familial acute myeloid leukaemia",
          "Pure familial acute myeloid leukemia",
          "familial AML",
          "hereditary acute myeloid leukaemia",
          "hereditary acute myeloid leukemia",
          "inherited AML"
        ],
        "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 instance of acute myeloid leukemia that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 6,
      "reference_id": "MONDO:0017893"
    },
    {
      "id": 20146,
      "label": "mixed phenotype acute leukemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19285
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017972",
          "MEDGEN:417342",
          "MedDRA:10067399",
          "NANDO:2200018",
          "NCIT:C82179",
          "Orphanet:530995",
          "UMLS:C2826025"
        ],
        "synonyms": [
          "MPAL",
          "mixed phenotype acute 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": "An acute leukemia of ambiguous lineage. It is characterized by the presence of either separate populations of blasts of more than one lineage, or one population of blasts co-expressing markers of more than one lineage."
      },
      "child_count": 3,
      "reference_id": "MONDO:0020743"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18103,
      "label": "inherited acute myeloid leukemia"
    },
    {
      "id": 20146,
      "label": "mixed phenotype acute leukemia"
    }
  ]
}