{
  "id": 10059,
  "label": "IRIDA syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008788",
  "properties": {
    "xrefs": [
      "GARD:0010957",
      "MEDGEN:39081",
      "MESH:C562385",
      "OMIM:206200",
      "Orphanet:209981",
      "SCTID:722005000",
      "UMLS:C0085576"
    ],
    "synonyms": [
      "IRIDA syndrome",
      "iron-refractory iron deficiency anaemia",
      "iron-refractory iron deficiency anemia",
      "IRIDA",
      "anemia, hypochromic microcytic, with defect in iron metabolism",
      "iron-handling disorder, hereditary",
      "pseudo-iron-deficiency Anaemia",
      "pseudo-iron-deficiency Anemia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "IRIDA (Iron-refractory iron deficiency anemia) syndrome is a rare autosomal recessive iron metabolism disorder characterized by iron deficiency anemia (hypochromic, microcytic) that is often unresponsive to oral iron intake and partially responsive to parenteral iron treatment."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3485,
      "label": "microcytic anemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4394
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11252",
          "HP:0001935",
          "MEDGEN:1673948",
          "NCIT:C35141",
          "SCTID:234349007",
          "UMLS:C5194182",
          "icd11.foundation:1380406043"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Anemia in which the red blood cell volume is decreased."
      },
      "child_count": 3,
      "reference_id": "MONDO:0001245"
    },
    {
      "id": 17107,
      "label": "hereditary anemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3835,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020669",
          "MEDGEN:1842172",
          "Orphanet:248296",
          "UMLS:C5680695"
        ],
        "synonyms": [
          "constitutional deficiency anemia",
          "constitutional rare deficiency anaemia",
          "constitutional rare deficiency anemia",
          "inherited deficiency anemia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 28,
      "reference_id": "MONDO:0016624"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3485,
      "label": "microcytic anemia"
    },
    {
      "id": 17107,
      "label": "hereditary anemia"
    }
  ]
}