{
  "id": 3185,
  "label": "hereditary spherocytosis type 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000913",
  "properties": {
    "xrefs": [
      "DOID:0110917",
      "GARD:0016149",
      "MEDGEN:436112",
      "OMIM:616649",
      "UMLS:C2674219"
    ],
    "synonyms": [
      "HS2",
      "SPH2",
      "SPTB hereditary spherocytosis",
      "hereditary spherocytosis caused by mutation in SPTB",
      "hereditary spherocytosis type 2",
      "spherocytosis, type 2",
      "spherocytosis, hereditary, 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Any hereditary spherocytosis in which the cause of the disease is a mutation in the SPTB gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19187,
      "label": "hereditary spherocytosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5573
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12971",
          "GARD:0006639",
          "ICD10CM:D58.0",
          "ICD9:282.0",
          "MEDGEN:52450",
          "MESH:D013103",
          "MedDRA:10019904",
          "NANDO:2200622",
          "NCIT:C97074",
          "NORD:777",
          "Orphanet:822",
          "SCTID:55995005",
          "UMLS:C0037889",
          "icd11.foundation:1305248013"
        ],
        "synonyms": [
          "Minkowski-Chauffard disease",
          "congenital spherocytic hemolytic anaemia",
          "hereditary spherocytosis",
          "spherocytic anaemia",
          "congenital spherocytosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum (from symptom-free carriers to severe hemolysis) characterized by anemia, variable jaundice, splenomegaly and cholelithiasis."
      },
      "child_count": 5,
      "reference_id": "MONDO:0019350"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19187,
      "label": "hereditary spherocytosis"
    }
  ]
}