{
  "id": 24287,
  "label": "HBA2-related alpha thalassemia spectrum",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100562",
  "properties": {
    "xrefs": [
      "GARD:0026281"
    ],
    "synonyms": [
      "alpha-thalassemia trait"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Mild microcytic anemia caused by biallelic variation in the HBA2 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24290,
      "label": "monogenic alpha thalassemia spectrum",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        12504
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026284"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "An instance of alpha thalessemia spectrum that is caused by an inherited monogenomic modification in an individual."
      },
      "child_count": 2,
      "reference_id": "MONDO:0100565"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24290,
      "label": "monogenic alpha thalassemia spectrum"
    }
  ]
}