{
  "id": 22049,
  "label": "monosomy 7 myelodysplasia and leukemia syndrome 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0030801",
  "properties": {
    "xrefs": [
      "GARD:0018506",
      "MEDGEN:1762901",
      "OMIM:619041",
      "UMLS:C5436668"
    ],
    "synonyms": [
      "M7MLS2",
      "monosomy 7 myelodysplasia and leukemia syndrome 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23376,
      "label": "familial monosomy 7 syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        18812
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020827",
          "MEDGEN:1826116",
          "OMIMPS:252270",
          "Orphanet:495930",
          "UMLS:C5681220"
        ],
        "synonyms": [
          "monosomy 7 myelodysplasia and leukaemia syndrome",
          "monosomy 7 myelodysplasia and leukemia syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A rare neoplastic disease characterized by infantile to childhood onset of evidence of bone marrow insufficiency/failure associated with increased risk for myelodysplastic syndrome or acute myeloid leukemia. Most patients present with petechiae, easy bruising, or anemia. Rapid progression is common, and prognosis is generally poor."
      },
      "child_count": 4,
      "reference_id": "MONDO:0044645"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23376,
      "label": "familial monosomy 7 syndrome"
    }
  ]
}