{
  "id": 3365,
  "label": "methemoglobinemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001117",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 23348,
      "label": "hemoglobinopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23347
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0044348"
    }
  ],
  "children": [
    {
      "id": 18710,
      "label": "drug-induced methemoglobinemia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3365,
        23349
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021930",
          "MEDGEN:632786",
          "NCIT:C101045",
          "Orphanet:464453",
          "SCTID:191390009",
          "UMLS:C0472781",
          "icd11.foundation:746336827"
        ],
        "synonyms": [
          "acquired methemoglobinemia",
          "drug induced methemoglobinemia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Methemoglobinemia that is caused by exposure to certain drugs (xylocaine and benzene)."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018740"
    },
    {
      "id": 18885,
      "label": "hereditary methemoglobinemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3365,
        4394,
        18953
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0002659",
          "ICD10CM:D74.0",
          "MEDGEN:473013",
          "MESH:C580280",
          "NCIT:C98898",
          "Orphanet:621",
          "SCTID:267550008",
          "UMLS:C0272087",
          "icd11.foundation:586921197"
        ],
        "synonyms": [
          "autosomal recessive methemoglobinemia",
          "congenital methemoglobinemia",
          "hereditary methemoglobinemia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Methemoglobinemia inherited in an autosomal recessive pattern. It is caused by deficiency of the enzyme NADH methemoglobin reductase or the presence of abnormal hemoglobin M. It presents with cyanosis early in life. There is no evidence of cardiopulmonary disease present."
      },
      "child_count": 15,
      "reference_id": "MONDO:0018963"
    }
  ],
  "roots": [
    {
      "id": 23348,
      "label": "hemoglobinopathy"
    }
  ]
}