{
  "id": 23348,
  "label": "hemoglobinopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0044348",
  "properties": {
    "xrefs": [
      "ICD9:282.7",
      "MEDGEN:42400",
      "SCTID:80141007",
      "UMLS:C0019045"
    ],
    "synonyms": [
      "hemoglobinopathy",
      "globin abnormality",
      "haemoglobin disease",
      "haemoglobin disorder",
      "hemoglobin disease",
      "hemoglobin disorder"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "id": 23347,
      "label": "erythrocyte disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7217
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:289.9",
          "MEDGEN:526127",
          "SCTID:38292009",
          "UMLS:C0221016"
        ],
        "synonyms": [
          "disease of erythrocyte",
          "disease or disorder of erythrocyte",
          "disorder of erythrocyte",
          "erythrocyte disease",
          "erythrocyte disease or disorder",
          "red blood cell disease",
          "red blood cell disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A disease or disorder that involves the erythrocyte."
      },
      "child_count": 2,
      "reference_id": "MONDO:0044347"
    }
  ],
  "children": [
    {
      "id": 3365,
      "label": "methemoglobinemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23348
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10783",
          "GARD:0022885",
          "ICD10CM:D74",
          "ICD9:289.7",
          "MEDGEN:6339",
          "MESH:D008708",
          "MedDRA:10027496",
          "NCIT:C34817",
          "SCTID:38959009",
          "UMLS:C0025637"
        ],
        "synonyms": [
          "methemoglobinemias"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "An inherited or acquired condition characterized by abnormally increased levels of methemoglobin in the blood."
      },
      "child_count": 2,
      "reference_id": "MONDO:0001117"
    },
    {
      "id": 8412,
      "label": "sulfhemoglobinemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23348
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12451",
          "EFO:1001200",
          "GARD:0024512",
          "MEDGEN:52562",
          "MESH:D013436",
          "MedDRA:10042481",
          "SCTID:32117000",
          "UMLS:C0038732"
        ],
        "synonyms": [
          "Sulfemoglobinemia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A morbid condition due to the presence of sulfmethemoglobin in the blood. It is marked by persistent cyanosis, but the blood count does not reveal any special abnormality in the blood. It is thought to be caused by the action of hydrogen sulfide absorbed from the intestine. (Stedman, 25th ed)"
      },
      "child_count": 1,
      "reference_id": "MONDO:0006988"
    },
    {
      "id": 18953,
      "label": "inherited hemoglobinopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        23348
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2860",
          "GARD:0018883",
          "ICD9:282.7",
          "MESH:D006453",
          "MedDRA:10060892",
          "NCIT:C3092",
          "Orphanet:68364",
          "SCTID:427306008"
        ],
        "synonyms": [
          "Hemoglobinopathies / iron metabolism",
          "hereditary hemoglobinopathy",
          "hemoglobinopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "An inherited disorder characterized by structural alterations of a globin chain within the hemoglobin molecule."
      },
      "child_count": 34,
      "reference_id": "MONDO:0019050"
    },
    {
      "id": 23349,
      "label": "acquired hemoglobinopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23348
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025903",
          "MEDGEN:688237",
          "SCTID:127039000",
          "UMLS:C1263995"
        ],
        "synonyms": [
          "acquired hemoglobinopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "An instance of hemoglobinopathy that is acquired during the lifetime of the individual."
      },
      "child_count": 1,
      "reference_id": "MONDO:0044349"
    }
  ],
  "roots": [
    {
      "id": 23347,
      "label": "erythrocyte disorder"
    }
  ]
}