{
  "id": 15126,
  "label": "congenital neutropenia-myelofibrosis-nephromegaly syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014118",
  "properties": {
    "xrefs": [
      "DOID:0112132",
      "GARD:0017585",
      "MEDGEN:815361",
      "OMIM:615285",
      "Orphanet:369852",
      "UMLS:C3809031"
    ],
    "synonyms": [
      "congenital neutropenia-bone marrow fibrosis-nephromegaly syndrome",
      "vps45 deficiency",
      "SCN5",
      "neutropenia, severe congenital, 5, autosomal recessive"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 21772,
      "label": "autosomal recessive severe congenital neutropenia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7611,
        18559
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021834",
          "MEDGEN:1781858",
          "NCIT:C176624",
          "Orphanet:439849",
          "UMLS:C5447331"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 12,
      "reference_id": "MONDO:0028226"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 21772,
      "label": "autosomal recessive severe congenital neutropenia"
    }
  ]
}