{
  "id": 14864,
  "label": "autosomal dominant aplasia and myelodysplasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013851",
  "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"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2750,
      "label": "bone marrow failure syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5177,
        5714
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 16,
      "reference_id": "MONDO:0000159"
    },
    {
      "id": 3901,
      "label": "inherited aplastic anemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        16610
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1342",
          "GARD:0018889",
          "ICD10CM:D61.0",
          "ICD9:284.0",
          "ICD9:284.09",
          "MEDGEN:1826154",
          "MESH:D029502",
          "NANDO:1200302",
          "NANDO:2201275",
          "Orphanet:397692",
          "Orphanet:68383",
          "SCTID:28975000",
          "UMLS:C5681331"
        ],
        "synonyms": [
          "constitutional aplastic anaemia",
          "constitutional aplastic anemia",
          "hereditary aplastic anaemia",
          "hereditary aplastic anemia",
          "rare constitutional aplastic anaemia",
          "rare constitutional aplastic anemia",
          "congenital aplastic anaemia",
          "congenital aplastic anemia",
          "congenital hypoplastic anaemia",
          "congenital hypoplastic anemia",
          "hypoplastic anaemia - familial",
          "hypoplastic anemia - familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "An inborn condition characterized by deficiencies of red cell precursors that sometimes also includes leukopenia and thrombocytopenia."
      },
      "child_count": 10,
      "reference_id": "MONDO:0001713"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2750,
      "label": "bone marrow failure syndrome"
    },
    {
      "id": 3901,
      "label": "inherited aplastic anemia"
    }
  ]
}