{
  "id": 8412,
  "label": "sulfhemoglobinemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0006988",
  "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)"
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "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": 9793,
      "label": "sulfhemoglobinemia, congenital",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8412,
        10564,
        18953
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024625",
          "MEDGEN:350024",
          "MESH:C566102",
          "OMIM:185460",
          "UMLS:C1861437"
        ],
        "synonyms": [
          "sulfhemoglobinemia, congenital"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0008502"
    }
  ],
  "roots": [
    {
      "id": 23348,
      "label": "hemoglobinopathy"
    }
  ]
}