{
  "id": 10566,
  "label": "hemolytic anemia with thermal sensitivity of red cells",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009334",
  "properties": {
    "xrefs": [
      "GARD:0015179",
      "MEDGEN:343488",
      "MESH:C565522",
      "OMIM:235370",
      "UMLS:C1856158"
    ],
    "synonyms": [
      "hemolytic anemia with thermal sensitivity of red cells"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17638,
      "label": "hereditary elliptocytosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5550
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2373",
          "GARD:0006621",
          "ICD10CM:D58.1",
          "MEDGEN:41747",
          "MESH:D004612",
          "MedDRA:10014490",
          "NANDO:2200630",
          "NCIT:C35882",
          "NORD:1935",
          "Orphanet:288",
          "SCTID:178935009",
          "UMLS:C0013902",
          "icd11.foundation:679955609"
        ],
        "synonyms": [
          "HE",
          "Hashimoto Encephalopathy",
          "congenital elliptocytosis",
          "hereditary ovalocytosis",
          "ovalocytosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Hereditary elliptocytosis (HE) is a rare clinically and genetically heterogeneous disorder of the red cell membrane characterized by manifestations ranging from mild to severe transfusion-dependent hemolytic anemia but with the majority of patients being asymptomatic."
      },
      "child_count": 5,
      "reference_id": "MONDO:0017319"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17638,
      "label": "hereditary elliptocytosis"
    }
  ]
}