{
  "id": 12488,
  "label": "dominant beta-thalassemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011381",
  "properties": {
    "xrefs": [
      "DOID:0080770",
      "GARD:0017164",
      "MEDGEN:347036",
      "MESH:C565834",
      "OMIM:603902",
      "Orphanet:231226",
      "SCTID:716682000",
      "UMLS:C1858990"
    ],
    "synonyms": [
      "inclusion body beta-thalassemia",
      "thalassemia-beta, dominant inclusion-body",
      "beta-thalassemia, dominant inclusion body type",
      "dyserythropoietic Anemia, congenital, Irish or Weatherall type"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Dominant beta-thalassemia is a form of beta-thalassemia resulting in moderate to severe anemia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19231,
      "label": "beta thalassemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3252,
        6875,
        17501
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12241",
          "GARD:0000871",
          "ICD10CM:D56.1",
          "ICD9:282.44",
          "ICD9:282.49",
          "MEDGEN:2611",
          "MESH:D017086",
          "MedDRA:10043391",
          "NANDO:2201274",
          "NCIT:C34375",
          "NORD:1765",
          "Orphanet:848",
          "SCTID:65959000",
          "UMLS:C0005283",
          "icd11.foundation:2063292324"
        ],
        "synonyms": [
          "Beta thalassemia intermedia",
          "Beta thalassemia minor",
          "Thalassemias, beta-",
          "erythroblastic anaemia",
          "erythroblastic anemia",
          "thalassemia major",
          "thalassemia, Hispanic gamma-delta-beta"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Beta-thalassemia (BT) is characterized by deficiency (Beta+) or absence (Beta0) of synthesis of the beta globin chains of hemoglobin (Hb)."
      },
      "child_count": 9,
      "reference_id": "MONDO:0019402"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19231,
      "label": "beta thalassemia"
    }
  ]
}