{
  "id": 3485,
  "label": "microcytic anemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001245",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 4394,
      "label": "anemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7217
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2355",
          "HP:0001903",
          "ICD9:285.8",
          "ICD9:285.9",
          "MEDGEN:1526",
          "MESH:D000740",
          "NCIT:C2869",
          "SCTID:271737000",
          "UMLS:C0002871"
        ],
        "synonyms": [
          "anaemia (disease)",
          "anemia",
          "anemia (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A reduction in the number of red blood cells, the amount of hemoglobin, and/or the volume of packed red blood cells. Clinically, anemia represents a reduction in the oxygen-transporting capacity of a designated volume of blood, resulting from an imbalance between blood loss (through hemorrhage or hemolysis) and blood production. Signs and symptoms of anemia may include pallor of the skin and mucous membranes, shortness of breath, palpitations of the heart, soft systolic murmurs, lethargy, and fatigability."
      },
      "child_count": 19,
      "reference_id": "MONDO:0002280"
    }
  ],
  "children": [
    {
      "id": 2886,
      "label": "hypochromic microcytic anemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3485,
        3581
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050642",
          "HP:0004840",
          "MEDGEN:124413",
          "MESH:C536357",
          "SCTID:44666001",
          "UMLS:C0271901"
        ],
        "synonyms": [
          "hypochromic microcytic anaemia (disease)",
          "hypochromic microcytic anemia",
          "hypochromic microcytic anemia (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Anemia in which the circulating RBCs are smaller than the usual size of RBCs (microcytic) and have decreased red color (hypochromic)."
      },
      "child_count": 4,
      "reference_id": "MONDO:0000387"
    },
    {
      "id": 8214,
      "label": "fetal erythroblastosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3485
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1098",
          "EFO:1000937",
          "GARD:0024468",
          "ICD9:773",
          "ICD9:773.2",
          "MEDGEN:4530",
          "MESH:D004899",
          "NCIT:C101304",
          "SCTID:387705004",
          "UMLS:C0014761"
        ],
        "synonyms": [
          "HDFN",
          "erythroblastosis fetalis",
          "hemolytic disease of the fetus or newborn",
          "hemolytic disease of the foetus or newborn",
          "hemolytic disease of the newborn",
          "isoimmune hemolytic disease of the newborn"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A disorder of the fetus or newborn that occurs when fetal cells that are coated with IgG alloantibodies from the mother attack antigens inherited from the father. Severity can range from absence of symptoms to death."
      },
      "child_count": 0,
      "reference_id": "MONDO:0006760"
    },
    {
      "id": 10059,
      "label": "IRIDA syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3485,
        17107
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008788"
    }
  ],
  "roots": [
    {
      "id": 4394,
      "label": "anemia"
    }
  ]
}