{
  "id": 2750,
  "label": "bone marrow failure syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000159",
  "properties": {
    "xrefs": [
      "GARD:0022719",
      "MEDGEN:419754",
      "MESH:C536572",
      "NCIT:C165614",
      "OMIMPS:614675",
      "UMLS:C2931245"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 8,
  "parents": [
    {
      "id": 5177,
      "label": "bone marrow disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6778,
        6893,
        7217
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4961",
          "GARD:0023414",
          "ICD9:289.9",
          "MEDGEN:892905",
          "MESH:D001855",
          "NCIT:C34433",
          "SCTID:127035006",
          "UMLS:C4021634"
        ],
        "synonyms": [
          "bone marrow disease",
          "bone marrow disease or disorder",
          "bone marrow disorder",
          "disease of bone marrow",
          "disease or disorder of bone marrow",
          "disorder of bone marrow"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Any disease of the bone marrow."
      },
      "child_count": 21,
      "reference_id": "MONDO:0003225"
    },
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    }
  ],
  "children": [
    {
      "id": 14864,
      "label": "autosomal dominant aplasia and myelodysplasia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2750,
        3901
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017420",
          "MEDGEN:814883",
          "NANDO:1200301",
          "OMIM:614675",
          "Orphanet:314399",
          "UMLS:C3808553"
        ],
        "synonyms": [
          "autosomal dominant aplastic anaemia and myelodysplasia",
          "autosomal dominant aplastic anemia and myelodysplasia",
          "bone marrow failure syndrome type 1",
          "BMFS1",
          "bone marrow failure syndrome 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013851"
    },
    {
      "id": 15320,
      "label": "pancytopenia-developmental delay syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2750,
        3901
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017655",
          "MEDGEN:816680",
          "OMIM:615715",
          "Orphanet:401764",
          "UMLS:C3810350"
        ],
        "synonyms": [
          "Trilineage bone marrow failure-developmental delay syndrome",
          "bone marrow failure syndrome type 2",
          "pancytopenia-developmental delay syndrome",
          "BMFS2",
          "bone marrow failure syndrome 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0014317"
    },
    {
      "id": 15868,
      "label": "bone marrow failure syndrome 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2750
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025030",
          "MEDGEN:934711",
          "OMIM:617052",
          "UMLS:C4310744"
        ],
        "synonyms": [
          "BMFS3",
          "DNAJC21 bone marrow failure syndrome",
          "DNAJC21-related bone marrow failure syndrome",
          "bone marrow failure syndrome 3",
          "bone marrow failure syndrome caused by mutation in DNAJC21",
          "bone marrow failure syndrome type 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Any bone marrow failure syndrome in which the cause of the disease is a mutation in the DNAJC21 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014887"
    },
    {
      "id": 20237,
      "label": "bone marrow failure syndrome 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2750
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025264",
          "MEDGEN:1648485",
          "OMIM:618116",
          "UMLS:C4748257"
        ],
        "synonyms": [
          "BMFS4",
          "BONE MARROW FAILURE SYNDROME 4"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020856"
    },
    {
      "id": 21802,
      "label": "bone marrow failure syndrome 6",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2750
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025508",
          "MEDGEN:1717739",
          "OMIM:618849",
          "UMLS:C5394274"
        ],
        "synonyms": [
          "BMFS6",
          "BONE MARROW FAILURE SYNDROME 6",
          "bone marrow failure syndrome 6"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030015"
    },
    {
      "id": 22101,
      "label": "AMED syndrome, digenic",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2750
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080952",
          "GARD:0018026",
          "MEDGEN:1754257",
          "OMIM:619151",
          "Orphanet:611216",
          "UMLS:C5436906"
        ],
        "synonyms": [
          "AMED syndrome, digenic",
          "AMEDS",
          "AMeD syndrome",
          "aplastic anemia-intellectual disability-dwarfism syndrome",
          "bone marrow failure syndrome 7, digenic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030894"
    },
    {
      "id": 22264,
      "label": "bone marrow failure syndrome 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2750
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025706",
          "MEDGEN:1648380",
          "OMIM:618165",
          "UMLS:C4748488"
        ],
        "synonyms": [
          "BMFS5",
          "BONE MARROW FAILURE SYNDROME 5"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032573"
    },
    {
      "id": 25735,
      "label": "Ziegler-Huang syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2750
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026870",
          "MEDGEN:1844409",
          "OMIM:620501",
          "UMLS:C5882688"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0957595"
    }
  ],
  "roots": [
    {
      "id": 5177,
      "label": "bone marrow disorder"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    }
  ]
}