{
  "id": 16998,
  "label": "delta-beta-thalassemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016489",
  "properties": {
    "xrefs": [
      "DOID:0080773",
      "GARD:0017165",
      "ICD10CM:D56.2",
      "ICD9:282.49",
      "MEDGEN:78790",
      "MESH:C562716",
      "MedDRA:10012236",
      "NCIT:C172823",
      "Orphanet:231237",
      "SCTID:16360009",
      "UMLS:C0271985"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Delta-beta-thalassemia is a form of beta-thalassemia characterized by decreased or absent synthesis of the delta- and beta-globin chains with a compensatory increase in expression of fetal gamma-chain synthesis."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17501,
      "label": "beta-thalassemia and related diseases",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4394,
        18953
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021023",
          "MEDGEN:1826095",
          "Orphanet:275749",
          "UMLS:C5680748"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 14,
      "reference_id": "MONDO:0017145"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17501,
      "label": "beta-thalassemia and related diseases"
    }
  ]
}