{
  "id": 24289,
  "label": "HBA1; HBA2-related digenic alpha thalassemia spectrum",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100564",
  "properties": {
    "xrefs": [
      "GARD:0026283"
    ],
    "synonyms": [
      "alpha-thalassemia trait"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Mild microcytic anemia caused by variation in two of the four copies of the alpha hemoglobin genes, which can be in cis (e.g., large deletion of HBA1 and HBA2 genes) or in trans (e.g., HBA1 variant on one chromosome and HBA2 variant on the other chromosome)."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24288,
      "label": "digenic alpha thalassemia spectrum",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        12504
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026282"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "An instance of alpha thalessemia spectrum that is caused by an inherited multiallelic modification in an individual."
      },
      "child_count": 3,
      "reference_id": "MONDO:0100563"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24288,
      "label": "digenic alpha thalassemia spectrum"
    }
  ]
}