{
  "id": 15792,
  "label": "sideroblastic anemia 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014804",
  "properties": {
    "xrefs": [
      "DOID:0080343",
      "GARD:0017235",
      "MEDGEN:895975",
      "OMIM:616860",
      "Orphanet:255132",
      "SCTID:720465002",
      "UMLS:C4225155"
    ],
    "synonyms": [
      "GLRX5-related sideroblastic anaemia",
      "GLRX5-related sideroblastic anemia",
      "SIDBA3",
      "adult-onset autosomal recessive sideroblastic anaemia",
      "adult-onset autosomal recessive sideroblastic anemia",
      "anemia, sideroblastic, 3, pyridoxine-refractory"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17234,
      "label": "mitochondrial substrate carrier disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17233
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020762",
          "MEDGEN:1842923",
          "Orphanet:254830",
          "UMLS:C5680716",
          "icd11.foundation:1118834100"
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0016801"
    },
    {
      "id": 17254,
      "label": "autosomal recessive sideroblastic anemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7611,
        19734
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017240",
          "MEDGEN:895586",
          "Orphanet:260305",
          "SCTID:717050005",
          "UMLS:C4274077"
        ],
        "synonyms": [
          "congenital sideroblastic anaemia",
          "congenital sideroblastic anemia",
          "ARSA",
          "sideroblastic anemia, autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Congenital autosomal recessive sideroblastic anemia (ARSA) is a non-syndromic, microcytic/hypochromic sideroblastic anemia, present from early infancy and characterized by severe microcytic anemia, which is not pyridoxine responsive, and increased serum ferritin."
      },
      "child_count": 4,
      "reference_id": "MONDO:0016828"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17234,
      "label": "mitochondrial substrate carrier disorder"
    },
    {
      "id": 17254,
      "label": "autosomal recessive sideroblastic anemia"
    }
  ]
}