{
  "id": 20127,
  "label": "X-linked sideroblastic anemia 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020721",
  "properties": {
    "xrefs": [
      "DOID:0060063",
      "GARD:0009456",
      "MEDGEN:1638704",
      "MESH:C536761",
      "OMIM:300751",
      "Orphanet:75563",
      "SCTID:62677000",
      "UMLS:C4551511"
    ],
    "synonyms": [
      "X-linked sideroblastic anemia",
      "XLSA",
      "anemia, sideroblastic, 1, X-linked recessive",
      "sideroblastic anemia, X-linked",
      "ANH1",
      "SIDBA1",
      "X chromosome-linked sideroblastic anaemia",
      "X chromosome-linked sideroblastic anemia",
      "anaemia hereditary sideroblastic",
      "anaemia sex-linked hypochromic sideroblastic",
      "anemia hereditary sideroblastic",
      "anemia sex-linked hypochromic sideroblastic",
      "anemia, hereditary sideroblastic",
      "anemia, hypochromic",
      "anemia, sideroblastic, 1",
      "anemia, sideroblastic, X-linked",
      "erythroid 5-aminolevulinate synthase deficiency",
      "hereditary iron-loading Anaemia",
      "hereditary iron-loading Anemia",
      "sideroblastic anaemia X-linked",
      "sideroblastic anemia X-linked"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2902,
      "label": "X-linked disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050735",
          "ICD9:799.89",
          "MEDGEN:222910",
          "MESH:D040181",
          "NCIT:C85865",
          "SCTID:128430005",
          "UMLS:C1138434"
        ],
        "synonyms": [
          "X-linked disease or disorder",
          "X-linked hereditary disease",
          "X-linked hereditary disorder",
          "X-linked inherited disease",
          "X-linked inherited disorder",
          "disease or disorder, X-linked",
          "disease, X-linked",
          "X linked genetic diseases",
          "X-linked genetic disease",
          "X-linked genetic diseases",
          "disease, X-linked genetic",
          "diseases, X-linked genetic",
          "genetic disease, X-linked",
          "genetic diseases, X chromosome linked",
          "genetic diseases, X linked",
          "genetic diseases, X-chromosome linked"
        ],
        "definition": "X-linked form of disease."
      },
      "child_count": 50,
      "reference_id": "MONDO:0000425"
    },
    {
      "id": 17981,
      "label": "inborn disorder of porphyrin metabolism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18954,
        22981
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021346",
          "Orphanet:309813",
          "SCTID:403832004"
        ],
        "synonyms": [
          "disorder of porphyrin and haem metabolism",
          "inborn disorder of porphyrin and haem metabolism",
          "inborn error of porphyrin-containing compound metabolic process",
          "inborn porphyrin-containing compound metabolic process disorder",
          "inherited disorder of porphyrin metabolism",
          "rare inborn error of porphyrin-containing compound metabolic process"
        ],
        "definition": "An inherited metabolic disease that is has its basis in the disruption of porphyrin-containing compound metabolic process."
      },
      "child_count": 8,
      "reference_id": "MONDO:0017754"
    },
    {
      "id": 19734,
      "label": "inherited sideroblastic anemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        16106
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019453",
          "MEDGEN:65119",
          "NANDO:1200892",
          "OMIMPS:300751",
          "Orphanet:98362",
          "UMLS:C0221018",
          "icd11.foundation:789053868"
        ],
        "synonyms": [
          "constitutional sideroblastic anaemia",
          "constitutional sideroblastic anemia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 16,
      "reference_id": "MONDO:0020099"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2902,
      "label": "X-linked disease"
    },
    {
      "id": 17981,
      "label": "inborn disorder of porphyrin metabolism"
    },
    {
      "id": 19734,
      "label": "inherited sideroblastic anemia"
    }
  ]
}