{
  "id": 10697,
  "label": "intrinsic factor and r binder, combined congenital deficiency of",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009471",
  "properties": {
    "xrefs": [
      "GARD:0015190",
      "MEDGEN:340942",
      "MESH:C565461",
      "OMIM:243320",
      "UMLS:C1855721"
    ],
    "synonyms": [
      "intrinsic factor and r binder, combined congenital deficiency of"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 11055,
      "label": "hereditary intrinsic factor deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17107,
        19087
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050734",
          "GARD:0003024",
          "ICD9:281.3",
          "MEDGEN:1876474",
          "MESH:C563242",
          "MedDRA:10070440",
          "OMIM:261000",
          "Orphanet:332",
          "SCTID:34925000",
          "SCTID:60504009",
          "UMLS:C2062370"
        ],
        "synonyms": [
          "intrinsic factor deficiency",
          "IFD",
          "congenital intrinsic factor deficiency",
          "congenital pernicious anaemia",
          "congenital pernicious anemia",
          "gastric intrinsic factor deficiency",
          "hereditary juvenile megaloblastic anaemia due to intrinsic factor deficiency",
          "hereditary juvenile megaloblastic anemia due to intrinsic factor deficiency",
          "congenital pernicious anaemia due to defect of intrinsic factor",
          "congenital pernicious anemia due to defect of intrinsic factor",
          "intrinsic factor, congenital deficiency of",
          "pernicious Anemia, congenital, due to defect of intrinsic Factor"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Congenital intrinsic factor deficiency (IFD) is a rare disorder of vitamin B12 (cobalamin) absorption that is characterized by megaloblastic anemia and neurological abnormalities."
      },
      "child_count": 2,
      "reference_id": "MONDO:0009852"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 11055,
      "label": "hereditary intrinsic factor deficiency"
    }
  ]
}