{
  "id": 9793,
  "label": "sulfhemoglobinemia, congenital",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008502",
  "properties": {
    "xrefs": [
      "GARD:0024625",
      "MEDGEN:350024",
      "MESH:C566102",
      "OMIM:185460",
      "UMLS:C1861437"
    ],
    "synonyms": [
      "sulfhemoglobinemia, congenital"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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": 10564,
      "label": "congenital hematological disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7217
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:760584",
          "NCIT:C104003",
          "UMLS:C3267032"
        ],
        "synonyms": [
          "congenital haematological system disease",
          "congenital hematological disorder",
          "congenital hematological system disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A disorder of the blood that is present at birth."
      },
      "child_count": 21,
      "reference_id": "MONDO:0009332"
    },
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8412,
      "label": "sulfhemoglobinemia"
    },
    {
      "id": 10564,
      "label": "congenital hematological disorder"
    },
    {
      "id": 18953,
      "label": "inherited hemoglobinopathy"
    }
  ]
}