{
  "id": 10058,
  "label": "microcytic anemia with liver iron overload",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008787",
  "properties": {
    "xrefs": [
      "GARD:0012360",
      "MEDGEN:812483",
      "OMIM:206100",
      "Orphanet:83642",
      "SCTID:711161006",
      "UMLS:C3806153"
    ],
    "synonyms": [
      "anemia, hypochromic microcytic, with iron overload type 1",
      "AHMIO1",
      "anemia, hypochromic microcytic, with iron overload 1",
      "hypochromic microcytic anaemia with iron overload",
      "hypochromic microcytic anemia with iron overload",
      "microcytic anaemia and hepatic iron overload",
      "microcytic anemia and hepatic iron overload"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "Congenital hypochromic microcytic anemia with progressive liver iron overload paradoxically associated with normal to moderately elevated serum ferritin levels has been described in three unrelated patients."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2723,
      "label": "anemia, hypochromic microcytic with iron overload",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2886,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022710",
          "MEDGEN:388759",
          "MESH:C567144",
          "OMIMPS:206100",
          "UMLS:C2673913"
        ],
        "synonyms": [
          "anemia, hypochromic microcytic, with iron overload"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0000104"
    },
    {
      "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"
    },
    {
      "id": 17988,
      "label": "disorder of iron metabolism and transport",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17986
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021355",
          "MEDGEN:1826109",
          "Orphanet:309842",
          "UMLS:C5681031"
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0017763"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2723,
      "label": "anemia, hypochromic microcytic with iron overload"
    },
    {
      "id": 17107,
      "label": "hereditary anemia"
    },
    {
      "id": 17988,
      "label": "disorder of iron metabolism and transport"
    }
  ]
}